Canonical Allele Identifier: PA1139711821
Gene: DNMT3B HGNC NCBI

Linked Data

ClinVar Variation Id: 952837
ClinVar RCV Id: RCV001225027
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008823.1:p.Val613Ala
CA408588429
NM_006892.4:c.1838T>C