Canonical Allele Identifier: PA645490646
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 392898
ClinVar RCV Id: RCV000420744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Cys5338Arg
CA16606557
NM_003482.4:c.16012T>C