GENETIC ENCYCLOPEDIA
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NM_000388.4(CASR):c.1629C>T (p.Ser543=) AND not provided

Significance: Uncertain significance
ClinVar: RCV000054617

Variant: NM_000388.4(CASR):c.1629C>T (p.Ser543=)

Type: Variant
Allele: NM_000388.4(CASR):c.1629C>T (p.Ser543=) 75395
Gene:
Type: single nucleotide variant
Location: Chr3: 122282133 - assembly GRCh38
Chr3: 122000980 - assembly GRCh37
References: dbSNP: 387907399

Condition

Disease: not provided