Canonical Allele Identifier: PA1139669921
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 943246
ClinVar RCV Id: RCV001213394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Ala301Thr
CA377510071
NM_000043.6:c.901G>A