Canonical Allele Identifier: PA915966870
Gene: KMT2B HGNC NCBI

Linked Data

ClinVar Variation Id: 692033
ClinVar RCV Id: RCV000853309
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055542.1:p.Cys1654Arg
CA405418832
NM_014727.3:c.4960T>C