Canonical Allele Identifier: PA126585
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 16505
ClinVar RCV Id: RCV000017969 RCV000638906 RCV001701481
JSON-LD

Amino-acid Alleles

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