Allele Registry

Canonical Allele Identifier: PA2826538511

Gene: AP3B1 HGNC NCBI

ClinVar RCV:

RCV000006744

ClinVar Variation:

6372

HGVS (amino-acid)	Matching Registered Transcripts
NP_001258698.1:p.Leu531Arg	CA340563 NM_001271769.2:c.1592T>G