Canonical Allele Identifier: PA126604
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 16513
ClinVar RCV Id: RCV000017977
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_690610.1:p.Gly226Ala
CA126602
NM_152871.4:c.677G>C