Canonical Allele Identifier: PA2741859597
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 2724049
ClinVar RCV Id: RCV003561571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304986.2:p.Glu556Asp
CA357854474
NM_001318057.2:c.1668A>T
CA357854475
NM_001318057.2:c.1668A>C