Allele Registry

Canonical Allele Identifier: PA133926

Gene: DSG2 HGNC NCBI

ClinVar Allele:

53465

ClinVar RCV:

RCV001056749

RCV001189712

RCV003996312

ClinVar Variation:

44298

HGVS (amino-acid)	Matching Registered Transcripts
NP_001934.2:p.Ala738Thr	CA021719 NM_001943.5:c.2212G>A