Canonical Allele Identifier: PA160740
Gene: KMT2C HGNC NCBI

Linked Data

ClinVar Variation Id: 134784

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733751.2:p.Asn3505Asp
CA160739
NM_170606.3:c.10513A>G