Canonical Allele Identifier: PA2826293812
Gene: DNMT3B HGNC NCBI

Linked Data

ClinVar Variation Id: 1059799
ClinVar RCV Id: RCV001369155
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193984.1:p.Pro145Arg
CA313185210
NM_001207055.1:c.434C>G