Canonical Allele Identifier: PA2825348117
Gene: CTNS HGNC NCBI

Linked Data

ClinVar Variation Id: 267310
ClinVar RCV Id: RCV000258031 RCV000691400 RCV002518787 RCV002051832
ClinVar Variation Id: 1455393
ClinVar RCV Id: RCV002569141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026851.2:p.Gly308Arg
CA8291955
NM_001031681.3:c.922G>A
CA397693194
NM_001031681.3:c.922G>C