Canonical Allele Identifier: PA2827353060
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 3235979
ClinVar RCV Id: RCV004555240

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317964.1:p.Asp517Gly
CA357854665
NM_001331035.2:c.1550A>G