Canonical Allele Identifier: PA2499299215
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1102504
ClinVar RCV Id: RCV001425845
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_690611.1:p.Thr220Ile
CA377509544
NM_152872.4:c.659C>T