Canonical Allele Identifier: PA2827445128
Gene: AP3B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1444913
ClinVar RCV Id: RCV001982650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335370.1:p.Asp93Asn
CA7699689
NM_001348441.2:c.277G>A