Canonical Allele Identifier: PA278066
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_001026851.2:p.Gly169Asp
CA278065
NM_001031681.3:c.506G>A