Canonical Allele Identifier: PA2499255333
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 1116399
ClinVar RCV Id: RCV001444740
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362207.1:p.Gln470His
CA3041927
NM_001375278.1:c.1410A>T
CA357856637
NM_001375278.1:c.1410A>C