Canonical Allele Identifier: PA645466197
Gene: FGA HGNC NCBI

Linked Data

ClinVar Variation Id: 347822
ClinVar RCV Id: RCV000344051 RCV000404726
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068657.1:p.Thr82Pro
CA3115349
NM_021871.4:c.244A>C