Allele Registry

Canonical Allele Identifier: PA658670740

Gene: DSG2 HGNC NCBI

ClinVar Allele:

469299

ClinVar RCV:

RCV000532176

ClinVar Variation:

466347

HGVS (amino-acid)	Matching Registered Transcripts
NP_001934.2:p.Thr191Ser	CA402133479 NM_001943.5:c.571A>T CA402133490 NM_001943.5:c.572C>G