Canonical Allele Identifier: PA2830300976
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1397440
ClinVar RCV Id: RCV001891705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_690610.1:p.Thr272Ile
CA377510020
NM_152871.4:c.815C>T