Canonical Allele Identifier: PA172433
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 158774
ClinVar RCV Id: RCV000146218
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Glu2007Ala
CA172432
NM_003482.4:c.6020A>C