Allele Registry

Canonical Allele Identifier: PA257639

Gene: DSG2 HGNC NCBI

ClinVar RCV:

RCV000018308

ClinVar Variation:

16815

HGVS (amino-acid)	Matching Registered Transcripts
NP_001934.2:p.Asn266Ser	CA022263 NM_001943.5:c.797A>G