Canonical Allele Identifier: PA1139713858
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 975279
ClinVar RCV Id: RCV001251821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Tyr5321Cys
CA384681773
NM_003482.4:c.15962A>G