Canonical Allele Identifier: PA645484964
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 322842
ClinVar RCV Id: RCV000284539 RCV000374508 RCV001274180 RCV002522942
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004928.2:p.Arg232His
CA8291860
NM_004937.3:c.695G>A