Canonical Allele Identifier: PA160684
Gene: KMT2C HGNC NCBI

Linked Data

ClinVar Variation Id: 134756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733751.2:p.Tyr2299Cys
CA160683
NM_170606.3:c.6896A>G