Canonical Allele Identifier: PA091559
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 16505
ClinVar RCV Id: RCV000017969 RCV000638906 RCV001701481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Arg250Pro
CA126583
NM_000043.6:c.749G>C