Canonical Allele Identifier: PA126580
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 16503

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_690610.1:p.Tyr211Cys
CA126578
NM_152871.4:c.632A>G