Canonical Allele Identifier: PA160598
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 134714
ClinVar RCV Id: RCV000121425 RCV001498479 RCV001818292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Pro4337Ala
CA160597
NM_003482.4:c.13009C>G