Canonical Allele Identifier: PA2828918939
Gene: FGB HGNC NCBI

Linked Data

ClinVar Variation Id: 16390
ClinVar RCV Id: RCV000017816
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369691.1:p.Gly330Asp
CA126444
NM_001382762.1:c.989G>A