Canonical Allele Identifier: PA2826219040
Gene: KMT2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2903788
ClinVar RCV Id: RCV003726910
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001184033.1:p.Leu2551Trp
CA6304417
NM_001197104.1:c.7652T>G