Canonical Allele Identifier: PA645458052
Gene: FASLG HGNC NCBI

Linked Data

ClinVar Variation Id: 293736
ClinVar RCV Id: RCV000329844 RCV004021376
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000630.1:p.His122Asn
CA1247528
NM_000639.3:c.364C>A