Canonical Allele Identifier: PA239237
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 193657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Pro790Ser
CA239236
NM_003482.4:c.2368C>T