Canonical Allele Identifier: PA2825204109
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 347827
ClinVar RCV Id: RCV000333369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000500.2:p.Ile413Val
CA10620302
NM_000509.5:c.1237A>G