Canonical Allele Identifier: PA2573159972
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1406333
ClinVar RCV Id: RCV001915774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Gln273Lys
CA377509878
NM_000043.6:c.817C>A