Canonical Allele Identifier: PA2828523727
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 4446
ClinVar RCV Id: RCV000004699 RCV002512764
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361424.1:p.Gly22Asp
CA278065
NM_001374495.1:c.65G>A