Canonical Allele Identifier: PA2829560451
Gene: AP3B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1444913
ClinVar RCV Id: RCV001982650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004635.2:p.Asp1030Asn
CA7699689
NM_004644.5:c.3088G>A