Allele Registry

Canonical Allele Identifier: PA1139720835

Gene: DSG2 HGNC NCBI

ClinVar RCV:

RCV001192254

ClinVar Variation:

928393

HGVS (amino-acid)	Matching Registered Transcripts
NP_001934.2:p.Ala358Pro	CA402138300 NM_001943.5:c.1072G>C