Canonical Allele Identifier: PA160656
Gene: KMT2C HGNC NCBI

Linked Data

ClinVar Variation Id: 134741
ClinVar RCV Id: RCV000121454 RCV003422000 RCV003133137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733751.2:p.Asn567Ser
CA160655
NM_170606.3:c.1700A>G