Canonical Allele Identifier: PA658809481
Gene: KMT2B HGNC NCBI

Linked Data

ClinVar Variation Id: 522861
ClinVar RCV Id: RCV000626041

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055542.1:p.Cys1644Phe
CA405418702
NM_014727.3:c.4931G>T