Canonical Allele Identifier: PA2828569168
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 1116399
ClinVar RCV Id: RCV001444740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362212.1:p.Gln443His
CA3041927
NM_001375283.1:c.1329A>T
CA357856637
NM_001375283.1:c.1329A>C