Canonical Allele Identifier: PA098137
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_004928.2:p.Gly110Val
CA116859
NM_004937.3:c.329G>T