Canonical Allele Identifier: PA160572
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 134702
ClinVar RCV Id: RCV000121412 RCV001289094 RCV001498880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Met2669Arg
CA160571
NM_003482.4:c.8006T>G