Allele Registry

Canonical Allele Identifier: PA113478

Gene: DSC2 HGNC NCBI

ClinVar RCV:

RCV000155026

RCV001065143

RCV004019075

ClinVar Variation:

72377

HGVS (amino-acid)	Matching Registered Transcripts
NP_077740.1:p.Arg203Cys	CA022869 NM_024422.6:c.607C>T