Canonical Allele Identifier: PA2828659297
Gene: DENND2B HGNC NCBI

Linked Data

ClinVar Variation Id: 218672
ClinVar RCV Id: RCV000203032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363427.1:p.Arg312Gln
CA249237
NM_001376498.1:c.935G>A