Canonical Allele Identifier: PA2573230725
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 1685551
ClinVar RCV Id: RCV002249278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Pro2020Ser
CA236612494
NM_003482.4:c.6058C>T