Canonical Allele Identifier: PA1139746710
Gene: DNMT3B HGNC NCBI

Linked Data

ClinVar Variation Id: 958456
ClinVar RCV Id: RCV001231627

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_787046.1:p.Ser207Arg
CA408586785
NM_175850.3:c.619A>C
CA408586795
NM_175850.3:c.621C>G
CA408586797
NM_175850.3:c.621C>A