Canonical Allele Identifier: PA2830300895
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1067934

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_690610.1:p.Asp239Asn
CA377509788
NM_152871.4:c.715G>A