Canonical Allele Identifier: PA271658
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 158784
ClinVar RCV Id: RCV000146231 RCV000516606 RCV001501756 RCV001657838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Pro2400Ala
CA271657
NM_003482.4:c.7198C>G