Canonical Allele Identifier: PA645489808
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 1420295
ClinVar RCV Id: RCV001914169
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Ser2719Thr
CA6546905
NM_003482.4:c.8156G>C