Canonical Allele Identifier: PA658679901
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 463013

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Ser59Gly
CA384689589
NM_003482.4:c.175A>G