Canonical Allele Identifier: PA645375412
Gene: KMT2B HGNC NCBI

Linked Data

ClinVar Variation Id: 430116
ClinVar RCV Id: RCV000493342
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055542.1:p.Pro2186Ala
CA405429273
NM_014727.3:c.6556C>G