Canonical Allele Identifier: PA1139712227
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 975418
ClinVar RCV Id: RCV001252034

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Thr1974Arg
CA384627519
NM_003482.4:c.5921C>G