Canonical Allele Identifier: PA160798
Gene: KMT2C HGNC NCBI

Linked Data

ClinVar Variation Id: 134814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733751.2:p.Pro4416Ser
CA160797
NM_170606.3:c.13246C>T