Canonical Allele Identifier: PA100395
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 66411
ClinVar RCV Id: RCV000056799 RCV001384253
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Asn116Ser
CA217067
NM_001927.4:c.347A>G