Canonical Allele Identifier: PA2828919052
Gene: FGB HGNC NCBI

Linked Data

ClinVar Variation Id: 1982341
ClinVar RCV Id: RCV002766704

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369693.1:p.Ser42Thr
CA358508247
NM_001382764.1:c.125G>C