Canonical Allele Identifier: PA217014
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 16832
ClinVar RCV Id: RCV000056771 RCV001316353
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Asn366del
CA217012
NM_001927.4:c.1097_1099del