Canonical Allele Identifier: PA2828523646
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_001361423.1:p.Gly161Arg
CA8291955
NM_001374494.1:c.481G>A
CA397693194
NM_001374494.1:c.481G>C