Canonical Allele Identifier: PA100117
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_005132.2:p.Arg196Cys
CA126446
NM_005141.5:c.586C>T