Canonical Allele Identifier: PA160528
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 134681

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Gly1849Glu
CA160527
NM_003482.4:c.5546G>A