Canonical Allele Identifier: PA2573230727
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 1368956
ClinVar RCV Id: RCV001894783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Asn2030Ser
CA384626697
NM_003482.4:c.6089A>G