Allele Registry

Canonical Allele Identifier: PA2830300960

Gene: FAS HGNC NCBI

ClinVar RCV:

RCV000337266

RCV003343765

ClinVar Variation:

301531

HGVS (amino-acid)	Matching Registered Transcripts
NP_690610.1:p.Glu268Asp	CA5593228 NM_152871.4:c.804A>C CA377509995 NM_152871.4:c.804A>T