Allele Registry

Canonical Allele Identifier: PA2828523206

Gene: CTNS HGNC NCBI

ClinVar RCV:

RCV000004708

RCV001193377

RCV001781181

RCV002512767

RCV003904807

ClinVar Variation:

4455

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361421.1:p.Gly339Arg	CA278067 NM_001374492.1:c.1015G>A CA397694169 NM_001374492.1:c.1015G>C