Canonical Allele Identifier: PA2825204112
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 347826

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000500.2:p.Gly429Trp
CA3115462
NM_000509.5:c.1285G>T