Allele Registry

Canonical Allele Identifier: PA133896

Gene: DSG2 HGNC NCBI

ClinVar RCV:

RCV000029667

RCV000037262

RCV000148472

RCV000472660

RCV000619528

RCV001081298

RCV001256759

ClinVar Variation:

36009

HGVS (amino-acid)	Matching Registered Transcripts
NP_001934.2:p.Val392Ile	CA021294 NM_001943.5:c.1174G>A