Canonical Allele Identifier: PA2573224240
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1464473
ClinVar RCV Id: RCV001997968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Thr17Ser
CA350682380
NM_001927.4:c.49A>T
CA350682390
NM_001927.4:c.50C>G