Canonical Allele Identifier: PA645384268
Gene: FGG HGNC NCBI

Linked Data

ClinVar Variation Id: 347827
ClinVar RCV Id: RCV000333369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068656.2:p.Ile413Val
CA10620302
NM_021870.3:c.1237A>G