Canonical Allele Identifier: PA2828569230
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 2724049
ClinVar RCV Id: RCV003561571

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362212.1:p.Glu529Asp
CA357854474
NM_001375283.1:c.1587A>T
CA357854475
NM_001375283.1:c.1587A>C