Allele Registry

Canonical Allele Identifier: PA1139721261

Gene: DSG2 HGNC NCBI

ClinVar RCV:

RCV001186572

ClinVar Variation:

924915

HGVS (amino-acid)	Matching Registered Transcripts
NP_001934.2:p.Cys507Ser	CA402141596 NM_001943.5:c.1519T>A CA402141601 NM_001943.5:c.1520G>C