Allele Registry

Canonical Allele Identifier: PA2825348117

Gene: CTNS HGNC NCBI

ClinVar RCV:

RCV000258031

RCV000691400

RCV002051832

RCV002518787

RCV002569141

ClinVar Variation:

267310

1455393

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