Canonical Allele Identifier: PA2828919029
Gene: FGB HGNC NCBI

Linked Data

ClinVar Variation Id: 3094592
ClinVar RCV Id: RCV004393929
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369692.1:p.Asp406Asn
CA358515582
NM_001382763.1:c.1216G>A