Canonical Allele Identifier: PA111233
Gene: DNMT3B HGNC NCBI

Linked Data

ClinVar Variation Id: 6740

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008823.1:p.Ala603Thr
CA118467
NM_006892.4:c.1807G>A