GENETIC ENCYCLOPEDIA
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NM_014633.5(CTR9):c.1126G>A (p.Glu376Lys) AND not specified

Significance: Uncertain significance
ClinVar: RCV000209881

Variant: NM_014633.5(CTR9):c.1126G>A (p.Glu376Lys)

Type: Variant
Allele: NM_014633.5(CTR9):c.1126G>A (p.Glu376Lys) 225883
Gene:
Type: single nucleotide variant
Location: Chr11: 10785358 - assembly GRCh37
Chr11: 10763811 - assembly GRCh38
References: dbSNP: 869312709

Condition

Disease: not specified