Canonical Allele Identifier: PA2830311143
Gene: CKAP2L HGNC NCBI

Linked Data

ClinVar Variation Id: 3145211
ClinVar RCV Id: RCV004444052
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689728.3:p.Thr211Ser
CA53691544
NM_152515.5:c.632C>G
CA348297793
NM_152515.5:c.631A>T