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NM_000388.4(CASR):c.1209T>C (p.Ser403=) AND not provided

Significance: Uncertain significance
ClinVar: RCV000054615

Variant: NM_000388.4(CASR):c.1209T>C (p.Ser403=)

Type: Variant
Allele: NM_000388.4(CASR):c.1209T>C (p.Ser403=) 75393
Gene:
Type: single nucleotide variant
Location: Chr3: 122262244 - assembly GRCh38
Chr3: 121981091 - assembly GRCh37
References: dbSNP: 387907400

Condition

Disease: not provided