Canonical Allele Identifier: PA126577
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 16502
ClinVar RCV Id: RCV000017966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_690611.1:p.Arg121Trp
CA126574
NM_152872.4:c.361C>T