Canonical Allele Identifier: PA160788
Gene: KMT2C HGNC NCBI

Linked Data

ClinVar Variation Id: 134809
ClinVar RCV Id: RCV000121522 RCV003133139
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733751.2:p.Met4124Val
CA160787
NM_170606.3:c.12370A>G