Allele Registry

Canonical Allele Identifier: PA100648

Gene: DSG2 HGNC NCBI

ClinVar RCV:

RCV000018307

RCV000037286

RCV000618751

RCV001183802

RCV002223761

RCV003914852

ClinVar Variation:

16814

HGVS (amino-acid)	Matching Registered Transcripts
NP_001934.2:p.Gly812Cys	CA021794 NM_001943.5:c.2434G>T