Canonical Allele Identifier: PA1139740788
Gene: KMT2B HGNC NCBI

Linked Data

ClinVar Variation Id: 932360
ClinVar RCV Id: RCV001200124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055542.1:p.Pro2110Leu
CA405427819
NM_014727.3:c.6329C>T