Canonical Allele Identifier: PA658680258
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 451141
ClinVar RCV Id: RCV000519625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Pro5285Arg
CA384683061
NM_003482.4:c.15854C>G