Canonical Allele Identifier: PA2830168332
Gene: UBE3B HGNC NCBI

Linked Data

ClinVar Variation Id: 1691089
ClinVar RCV Id: RCV002254001

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_569733.2:p.Gly779Arg
CA386643448
NM_130466.4:c.2335G>A
CA386643450
NM_130466.4:c.2335G>C