Canonical Allele Identifier: PA2828568940
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 347156
ClinVar RCV Id: RCV000325590 RCV002294306 RCV001512909 RCV001528675 RCV002520195 RCV001849181 RCV003224266
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362211.1:p.Lys434Arg
CA3041942
NM_001375282.1:c.1301A>G