Canonical Allele Identifier: PA645430521
Gene: CLPTM1L HGNC NCBI

Linked Data

ClinVar Variation Id: 402547
ClinVar RCV Id: RCV000454864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110409.2:p.Val74Leu
CA16609726
NM_030782.5:c.220G>C