Canonical Allele Identifier: PA1139669886
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 848671
ClinVar RCV Id: RCV001052481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Thr235del
CA916080420
NM_000043.6:c.704_706del