Canonical Allele Identifier: PA2825204098
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 2573605
ClinVar RCV Id: RCV003317941
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000500.2:p.Gly377Val
CA3115481
NM_000509.5:c.1130G>T