Canonical Allele Identifier: PA2828569226
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 2891695
ClinVar RCV Id: RCV003725072

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362212.1:p.Gly523Ser
CA3041853
NM_001375283.1:c.1567G>A