Canonical Allele Identifier: PA2580364070
Gene: KMT2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1720216
ClinVar RCV Id: RCV002298009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055542.1:p.Pro2351Ser
CA405431465
NM_014727.3:c.7051C>T