Allele Registry

Canonical Allele Identifier: PA2828523948

Gene: CTNS HGNC NCBI

ClinVar Allele:

34291

ClinVar RCV:

RCV000020624

RCV001276660

RCV001781295

RCV002243657

RCV002513140

ClinVar Variation:

21439

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361425.1:p.Leu11Pro	CA342075 NM_001374496.1:c.32T>C