Canonical Allele Identifier: PA109151
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 16362
ClinVar RCV Id: RCV000017777 RCV000851952 RCV002225266 RCV003151729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068656.2:p.Arg301His
CA126391
NM_021870.3:c.902G>A