Canonical Allele Identifier: PA271651
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 158777

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Ala2214Thr
CA271650
NM_003482.4:c.6640G>A