Canonical Allele Identifier: PA111319
Gene: DNMT3B HGNC NCBI

Linked Data

ClinVar Variation Id: 2138340
ClinVar RCV Id: RCV003050554

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008823.1:p.Val606Ala
CA313155126
NM_006892.4:c.1817T>C