Canonical Allele Identifier: PA2828918658
Gene: FGB HGNC NCBI

Linked Data

ClinVar Variation Id: 16395
ClinVar RCV Id: RCV000017821
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369688.1:p.Leu158Gln
CA126450
NM_001382759.1:c.473T>A