Canonical Allele Identifier: PA2741901500
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 2845016
ClinVar RCV Id: RCV003754621

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Ser2719Gly
CA384743748
NM_003482.4:c.8155A>G