Canonical Allele Identifier: PA205822
Gene: EHMT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 210922
ClinVar RCV Id: RCV000192769 RCV001045045
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079033.4:p.Ala947Thr
CA205821
NM_024757.5:c.2839G>A