Canonical Allele Identifier: PA206527
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 211316
ClinVar RCV Id: RCV000193203 RCV001852558 RCV003389759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Met3881Val
CA206526
NM_003482.4:c.11641A>G