Allele Registry

Canonical Allele Identifier: PA100386

Gene: DES HGNC NCBI

ClinVar RCV:

RCV000056789

RCV000155027

RCV000498999

RCV000684771

RCV000844627

RCV002381360

ClinVar Variation:

66402

HGVS (amino-acid)	Matching Registered Transcripts
NP_001918.3:p.Arg454Trp	CA217043 NM_001927.4:c.1360C>T