Canonical Allele Identifier: PA174463
Gene: AP3B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 161617
ClinVar RCV Id: RCV000149153 RCV001850022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003655.3:p.Arg509Gln
CA174461
NM_003664.5:c.1526G>A