Canonical Allele Identifier: PA2828918684
Gene: FGB HGNC NCBI

Linked Data

ClinVar Variation Id: 16383
ClinVar RCV Id: RCV000017807
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369688.1:p.Ala321Thr
CA126431
NM_001382759.1:c.961G>A