Canonical Allele Identifier: PA645489238
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 309061
ClinVar RCV Id: RCV001002444 RCV001859848
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Gly1622Ala
CA6547698
NM_003482.4:c.4865G>C