Canonical Allele Identifier: PA091573
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 16506
ClinVar RCV Id: RCV000017970 RCV001851899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Thr270Ile
CA126586
NM_000043.6:c.809C>T