Canonical Allele Identifier: PA217074
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 66413
ClinVar RCV Id: RCV000056802 RCV000239680
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Arg16Cys
CA217072
NM_001927.4:c.46C>T