Canonical Allele Identifier: PA916053591
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 16508
ClinVar RCV Id: RCV000017972
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_690611.1:p.Ala25Thr
CA212971
NM_152872.4:c.73G>A