Canonical Allele Identifier: PA2580193075
Gene: CKAP2L HGNC NCBI

Linked Data

ClinVar Variation Id: 2411628
ClinVar RCV Id: RCV002779798

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291290.1:p.Met1Ile
CA53691718
NM_001304361.2:c.3G>T
CA348298097
NM_001304361.2:c.3G>C
CA348298098
NM_001304361.2:c.3G>A