Canonical Allele Identifier: PA2825204106
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 1098506
ClinVar RCV Id: RCV001420439
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000500.2:p.Arg401Gln
CA358535343
NM_000509.5:c.1202G>A