Allele Registry

Canonical Allele Identifier: PA2828915996

Gene: DES HGNC NCBI

ClinVar RCV:

RCV001977351

ClinVar Variation:

1473035

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369639.1:p.Ala337Ser	CA350693316 NM_001382710.1:c.1009G>T