Canonical Allele Identifier: PA2830300992
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 943246
ClinVar RCV Id: RCV001213394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_690610.1:p.Ala280Thr
CA377510071
NM_152871.4:c.838G>A