Allele Registry

Canonical Allele Identifier: PA126569

Gene: FAS HGNC NCBI

ClinVar RCV:

RCV000017963

ClinVar Variation:

16499

HGVS (amino-acid)	Matching Registered Transcripts
NP_690610.1:p.Thr220Pro	CA126567 NM_152871.4:c.658A>C