Canonical Allele Identifier: PA2499227039
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1055284
ClinVar RCV Id: RCV001363929
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Val254Phe
CA377509739
NM_000043.6:c.760G>T