Canonical Allele Identifier: PA913195925
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 598764
ClinVar RCV Id: RCV000735232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.His1405Arg
CA384649167
NM_003482.4:c.4214A>G