Canonical Allele Identifier: PA2828569214
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 12122
ClinVar RCV Id: RCV000012905

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362212.1:p.Asp505Val
CA256214
NM_001375283.1:c.1514A>T