Canonical Allele Identifier: PA126392
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 16362
ClinVar RCV Id: RCV000017777 RCV000851952 RCV002225266 RCV003151729
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000500.2:p.Arg301His
CA126391
NM_000509.5:c.902G>A