Allele Registry

Canonical Allele Identifier: PA2828523272

Gene: CTNS HGNC NCBI

ClinVar RCV:

RCV000258035

RCV002519021

ClinVar Variation:

267308

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361422.1:p.Trp35Arg	CA8291771 NM_001374493.1:c.103T>C CA397691384 NM_001374493.1:c.103T>A