Canonical Allele Identifier: PA2825084101
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 1721564
ClinVar RCV Id: RCV002300521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000195.3:p.Asn564Lys
CA357854293
NM_000204.5:c.1692T>G
CA357854294
NM_000204.5:c.1692T>A