Canonical Allele Identifier: PA2741945370
Gene: KMT2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2976716
ClinVar RCV Id: RCV003838850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055542.1:p.Tyr1671Cys
CA405419094
NM_014727.3:c.5012A>G