Canonical Allele Identifier: PA2829549592
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_004928.2:p.Arg63His
CA8291599
NM_004937.3:c.188G>A