Canonical Allele Identifier: PA645498427
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 287812

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Pro419Leu
CA10605881
NM_001927.4:c.1256C>T