Allele Registry

Canonical Allele Identifier: PA2828915588

Gene: DES HGNC NCBI

ClinVar RCV:

RCV001249249

ClinVar Variation:

972950

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369638.1:p.Arg262Leu	CA350695018 NM_001382709.1:c.785G>T