Canonical Allele Identifier: PA126422
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 16378
ClinVar RCV Id: RCV000017800 RCV000791084 RCV000851827 RCV000963143 RCV001144043 RCV002222000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000500.2:p.Gly191Arg
CA126421
NM_000509.5:c.571G>A
CA358536807
NM_000509.5:c.571G>C