Canonical Allele Identifier: PA126569
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 16499
ClinVar RCV Id: RCV000017963
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_690610.1:p.Thr220Pro
CA126567
NM_152871.4:c.658A>C