Canonical Allele Identifier: PA658810028
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 500446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Ile2026Val
CA6547378
NM_003482.4:c.6076A>G