Canonical Allele Identifier: PA2830300880
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1715761
ClinVar RCV Id: RCV002301488
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_690610.1:p.Lys237Glu
CA377509774
NM_152871.4:c.709A>G