Canonical Allele Identifier: PA2828569181
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 347153
ClinVar RCV Id: RCV000322070 RCV001753817
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362212.1:p.Asp458His
CA3041918
NM_001375283.1:c.1372G>C