Canonical Allele Identifier: PA116860
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 4457
ClinVar RCV Id: RCV000004710
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026851.2:p.Gly110Val
CA116859
NM_001031681.3:c.329G>T