Canonical Allele Identifier: PA2825204102
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 2683318
ClinVar RCV Id: RCV003480138
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000500.2:p.Asn391Ile
CA358535409
NM_000509.5:c.1172A>T