Canonical Allele Identifier: PA2828523479
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_001361423.1:p.Ser7Arg
CA8291717
NM_001374494.1:c.19A>C
CA8291752
NM_001374494.1:c.21T>G
CA397691217
NM_001374494.1:c.21T>A