Canonical Allele Identifier: PA2829549671
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 1981332
ClinVar RCV Id: RCV002751414
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004928.2:p.Ser154Arg
CA8291717
NM_004937.3:c.460A>C
CA8291752
NM_004937.3:c.462T>G
CA397691217
NM_004937.3:c.462T>A