Allele Registry

Canonical Allele Identifier: PA645498160

Gene: DES HGNC NCBI

ClinVar RCV:

RCV000227930

ClinVar Variation:

239071

HGVS (amino-acid)	Matching Registered Transcripts
NP_001918.3:p.Leu338Pro	CA10581950 NM_001927.4:c.1013T>C