Canonical Allele Identifier: PA126433
Gene: FGB HGNC NCBI

Linked Data

ClinVar Variation Id: 16383
ClinVar RCV Id: RCV000017807

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005132.2:p.Ala365Thr
CA126431
NM_005141.5:c.1093G>A