Allele Registry

Canonical Allele Identifier: PA658831795

Gene: KMT2B HGNC NCBI

ClinVar Variation Id: 549479

HGVS (amino-acid)	Matching Registered Transcripts
NP_055542.1:p.Phe1662Leu	CA405418935 NM_014727.3:c.4984T>C CA405418948 NM_014727.3:c.4986C>A CA405418950 NM_014727.3:c.4986C>G