Canonical Allele Identifier: PA2826294226
Gene: DNMT3B HGNC NCBI

Linked Data

ClinVar Variation Id: 1716279
ClinVar RCV Id: RCV002303357
ClinVar Variation Id: 3084820
ClinVar RCV Id: RCV004381683

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193985.1:p.Gln121His
CA9810260
NM_001207056.1:c.363G>T
CA408586825
NM_001207056.1:c.363G>C