Allele Registry

Canonical Allele Identifier: PA2827027392

Gene: DSP HGNC NCBI

ClinVar RCV:

RCV003789833

RCV004005997

ClinVar Variation:

2930523

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305963.1:p.His371Leu	CA362675719 NM_001319034.2:c.1112A>T