Canonical Allele Identifier: PA2580193076
Gene: CKAP2L HGNC NCBI

Linked Data

ClinVar Variation Id: 2295354
ClinVar RCV Id: RCV002865250
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291290.1:p.Leu23Phe
CA348297943
NM_001304361.2:c.69G>T
CA348297944
NM_001304361.2:c.69G>C