Canonical Allele Identifier: PA2573196052
Gene: CKAP2L HGNC NCBI

Linked Data

ClinVar Variation Id: 1358558
ClinVar RCV Id: RCV001864113
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291290.1:p.Pro36Ala
CA1836819
NM_001304361.2:c.106C>G