Canonical Allele Identifier: PA160590
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 134710
ClinVar RCV Id: RCV000121421 RCV000726604 RCV001501324
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Arg3656Cys
CA160589
NM_003482.4:c.10966C>T