Allele Registry

Canonical Allele Identifier: PA2580183049

Gene: CASP7 HGNC NCBI

ClinVar RCV:

RCV004197997

ClinVar Variation:

2357284

HGVS (amino-acid)	Matching Registered Transcripts
NP_001253986.1:p.Cys256Ser	CA5696387 NM_001267057.1:c.767G>C CA378422766 NM_001267057.1:c.766T>A