Canonical Allele Identifier: PA2828522926
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 3078700
ClinVar RCV Id: RCV004374989
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361421.1:p.Arg63His
CA8291599
NM_001374492.1:c.188G>A