Canonical Allele Identifier: PA916028668
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 66014
ClinVar RCV Id: RCV000056257 RCV000056258 RCV001439482 RCV001328281 RCV003147337
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317964.1:p.Gly119Arg
CA278398
NM_001331035.2:c.355G>A
CA357864123
NM_001331035.2:c.355G>C