Allele Registry

Canonical Allele Identifier: PA353886

Gene: DSC2 HGNC NCBI

ClinVar RCV:

RCV000208003

RCV001303072

RCV003997671

ClinVar Variation:

222557

HGVS (amino-acid)	Matching Registered Transcripts
NP_004940.1:p.Thr275Met	CA040141 NM_004949.5:c.824C>T