Allele Registry

Canonical Allele Identifier: PA133888

Gene: DES HGNC NCBI

ClinVar RCV:

RCV000037258

RCV000243219

RCV000725547

RCV001085666

RCV003914934

ClinVar Variation:

44275

HGVS (amino-acid)	Matching Registered Transcripts
NP_001918.3:p.Asp312Ala	CA133886 NM_001927.4:c.935A>C