Canonical Allele Identifier: PA2828523567
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_001361423.1:p.Arg85His
CA8291860
NM_001374494.1:c.254G>A