Canonical Allele Identifier: PA2825204099
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 2682873
ClinVar RCV Id: RCV003481740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000500.2:p.Tyr380Asn
CA358535485
NM_000509.5:c.1138T>A