Canonical Allele Identifier: PA2826538466
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_001258698.1:p.Arg460Gln
CA174461
NM_001271769.2:c.1379G>A