Canonical Allele Identifier: PA658810107
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 500417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Pro3129Ser
CA6546701
NM_003482.4:c.9385C>T