Canonical Allele Identifier: PA170902
Gene: DLX5 HGNC NCBI

Linked Data

ClinVar Variation Id: 91861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005212.1:p.Gln186His
CA170901
NM_005221.6:c.558G>T
CA368261243
NM_005221.6:c.558G>C