Canonical Allele Identifier: PA2499279149
Gene: KMT2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1031844
ClinVar RCV Id: RCV001333776
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055542.1:p.Ala1669Val
CA405419055
NM_014727.3:c.5006C>T