Canonical Allele Identifier: PA2580198934
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 1721564
ClinVar RCV Id: RCV002300521
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304986.2:p.Asn572Lys
CA357854293
NM_001318057.2:c.1716T>G
CA357854294
NM_001318057.2:c.1716T>A