Canonical Allele Identifier: PA2580363970
Gene: KMT2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2049559
ClinVar RCV Id: RCV002937157

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055542.1:p.Ala2010Ser
CA9385586
NM_014727.3:c.6028G>T