Canonical Allele Identifier: PA160790
Gene: KMT2C HGNC NCBI

Linked Data

ClinVar Variation Id: 134810
ClinVar RCV Id: RCV000121523 RCV001854658 RCV002505064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733751.2:p.Ile237Val
CA160789
NM_170606.3:c.709A>G