Canonical Allele Identifier: PA645511262
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 438838
ClinVar RCV Id: RCV000505820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Ser42Phe
CA384690291
NM_003482.4:c.125C>T