Canonical Allele Identifier: PA2828918893
Gene: FGB HGNC NCBI

Linked Data

ClinVar Variation Id: 16387
ClinVar RCV Id: RCV000017811
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369691.1:p.Ala98Thr
CA126440
NM_001382762.1:c.292G>A