Allele Registry

Canonical Allele Identifier: PA181191

Gene: DES HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000154696

RCV000157163

RCV000229797

RCV000307432

RCV000393436

RCV000406154

RCV000725364

RCV001264391

RCV001798502

RCV002362812

ClinVar Variation:

178015

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001918.3:p.Arg212Gln	CA181189 NM_001927.4:c.635G>A