Canonical Allele Identifier: PA109192
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 16370
ClinVar RCV Id: RCV000017790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068656.2:p.Asp356Val
CA126408
NM_021870.3:c.1067A>T