Canonical Allele Identifier: PA1139740793
Gene: KMT2B HGNC NCBI

Linked Data

ClinVar Variation Id: 916169
ClinVar RCV Id: RCV001171702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055542.1:p.Pro2221Ser
CA405429758
NM_014727.3:c.6661C>T