Canonical Allele Identifier: PA2826889649
Gene: CKAP2L HGNC NCBI

Linked Data

ClinVar Variation Id: 1030263
ClinVar RCV Id: RCV001331777 RCV002546508
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291290.1:p.Glu297Val
CA1836672
NM_001304361.2:c.890A>T