Canonical Allele Identifier: PA2825347868
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 1981332
ClinVar RCV Id: RCV002751414
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026851.2:p.Ser154Arg
CA8291717
NM_001031681.3:c.460A>C
CA8291752
NM_001031681.3:c.462T>G
CA397691217
NM_001031681.3:c.462T>A