Canonical Allele Identifier: PA174903
Gene: CADPS HGNC NCBI

Linked Data

ClinVar Variation Id: 161849
ClinVar RCV Id: RCV000149385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_899630.1:p.Ala162Thr
CA174902
NM_183393.3:c.484G>A