Canonical Allele Identifier: PA2829361631
Gene: DLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2066999

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001925.2:p.Ser131Thr
CA291490593
NM_001934.4:c.391T>A