Allele Registry

Canonical Allele Identifier: PA126585

Gene: FAS HGNC NCBI

ClinVar Allele:

31544

ClinVar RCV:

RCV000017969

RCV000638906

RCV001701481

ClinVar Variation:

16505

HGVS (amino-acid)	Matching Registered Transcripts
NP_690610.1:p.Arg229Pro	CA126583 NM_152871.4:c.686G>C