Allele Registry

Canonical Allele Identifier: PA100657

Gene: DSG2 HGNC NCBI

ClinVar RCV:

RCV000037261

RCV000157183

RCV000252861

RCV000656843

RCV000777939

RCV001034652

RCV003224120

ClinVar Variation:

44278

HGVS (amino-acid)	Matching Registered Transcripts
NP_001934.2:p.Thr335Ala	CA021231 NM_001943.5:c.1003A>G