Canonical Allele Identifier: PA645384243
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 432325
ClinVar RCV Id: RCV000497584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068656.2:p.Lys238Arg
CA358536471
NM_021870.3:c.713A>G