Canonical Allele Identifier: PA645489971
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 376901
ClinVar RCV Id: RCV000436939 RCV002061318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Met3398Leu
CA6546590
NM_003482.4:c.10192A>C
CA384731763
NM_003482.4:c.10192A>T