Canonical Allele Identifier: PA645384286
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 347826
ClinVar RCV Id: RCV000259529 RCV002520216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068656.2:p.Gly429Trp
CA3115462
NM_021870.3:c.1285G>T