Canonical Allele Identifier: PA2828918717
Gene: FGB HGNC NCBI

Linked Data

ClinVar Variation Id: 1982341
ClinVar RCV Id: RCV002766704

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369689.1:p.Ser42Thr
CA358508247
NM_001382760.1:c.125G>C