Canonical Allele Identifier: PA2826294131
Gene: DNMT3B HGNC NCBI

Linked Data

ClinVar Variation Id: 6734

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193984.1:p.Val693Met
CA118461
NM_001207055.1:c.2077G>A