Canonical Allele Identifier: PA916019354
Gene: FASLG HGNC NCBI

Linked Data

ClinVar Variation Id: 293734
ClinVar RCV Id: RCV000356098
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289675.1:p.Ala93Val
CA1247494
NM_001302746.2:c.278C>T