Allele Registry

Canonical Allele Identifier: PA308271

Gene: DES HGNC NCBI

ClinVar RCV:

RCV000183352

RCV000459000

RCV001798637

ClinVar Variation:

201705

HGVS (amino-acid)	Matching Registered Transcripts
NP_001918.3:p.His326Tyr	CA308269 NM_001927.4:c.976C>T