Canonical Allele Identifier: PA2830311135
Gene: CKAP2L HGNC NCBI

Linked Data

ClinVar Variation Id: 2411628
ClinVar RCV Id: RCV002779798

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689728.3:p.Met166Ile
CA53691718
NM_152515.5:c.498G>T
CA348298097
NM_152515.5:c.498G>C
CA348298098
NM_152515.5:c.498G>A