Canonical Allele Identifier: PA2580313959
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 2145535
ClinVar RCV Id: RCV003071485
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004928.2:p.Met287Thr
CA8291941
NM_004937.3:c.860T>C