Canonical Allele Identifier: PA2827353082
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_001317964.1:p.Asn557Lys
CA357854293
NM_001331035.2:c.1671T>G
CA357854294
NM_001331035.2:c.1671T>A