Canonical Allele Identifier: PA2828918959
Gene: FGB HGNC NCBI

Linked Data

ClinVar Variation Id: 16382

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369692.1:p.Arg44Cys
CA126428
NM_001382763.1:c.130C>T