Canonical Allele Identifier: PA174762
Gene: CLPTM1L HGNC NCBI

Linked Data

ClinVar Variation Id: 161775
ClinVar RCV Id: RCV000149311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110409.2:p.Arg250His
CA174761
NM_030782.5:c.749G>A