Canonical Allele Identifier: PA2828919085
Gene: FGB HGNC NCBI

Linked Data

ClinVar Variation Id: 16391
ClinVar RCV Id: RCV000017817 RCV000851604
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369693.1:p.Arg196Cys
CA126446
NM_001382764.1:c.586C>T