Canonical Allele Identifier: PA163331
Gene: DNMT3A HGNC NCBI

Linked Data

ClinVar Variation Id: 139619
ClinVar RCV Id: RCV000128562
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_783328.1:p.Phe902Ser
CA163326
NM_175629.2:c.2705T>C