Allele Registry

Canonical Allele Identifier: PA2826281137

Gene: CASP7 HGNC NCBI

ClinVar RCV:

RCV004197997

ClinVar Variation:

2357284

HGVS (amino-acid)	Matching Registered Transcripts
NP_001218.1:p.Cys171Ser	CA5696387 NM_001227.5:c.512G>C CA378422766 NM_001227.5:c.511T>A