Canonical Allele Identifier: PA2825347760
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 1210394
ClinVar RCV Id: RCV001580688 RCV001580689 RCV001580690 RCV002573265
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026851.2:p.Arg63Cys
CA8291597
NM_001031681.3:c.187C>T