Canonical Allele Identifier: PA100784
Gene: DLX5 HGNC NCBI

Linked Data

ClinVar Variation Id: 30021
ClinVar RCV Id: RCV000022921
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005212.1:p.Gln178Pro
CA128834
NM_005221.6:c.533A>C