Canonical Allele Identifier: PA160562
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 134697
ClinVar RCV Id: RCV000121407 RCV000659757 RCV000945876 RCV001657764 RCV003224159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Gly2569Ser
CA160561
NM_003482.4:c.7705G>A