Canonical Allele Identifier: PA2828918865
Gene: FGB HGNC NCBI

Linked Data

ClinVar Variation Id: 16389
ClinVar RCV Id: RCV000017815
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369690.1:p.Leu383Arg
CA126442
NM_001382761.1:c.1148T>G