Canonical Allele Identifier: PA2828569210
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 1431614
ClinVar RCV Id: RCV001967578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362212.1:p.Gly497Val
CA3041862
NM_001375283.1:c.1490G>T