Allele Registry

Canonical Allele Identifier: PA126604

Gene: FAS HGNC NCBI

ClinVar RCV:

RCV000017977

ClinVar Variation:

16513

HGVS (amino-acid)	Matching Registered Transcripts
NP_690610.1:p.Gly226Ala	CA126602 NM_152871.4:c.677G>C