Canonical Allele Identifier: PA160592
Gene: KMT2D HGNC NCBI

Linked Data

ClinVar Variation Id: 134711
ClinVar RCV Id: RCV000121422 RCV000146150 RCV000377054 RCV000513704
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003473.3:p.Pro3665Ala
CA160591
NM_003482.4:c.10993C>G