Canonical Allele Identifier: PA2825347762
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_001026851.2:p.Arg63His
CA8291599
NM_001031681.3:c.188G>A