Canonical Allele Identifier: PA2826538521
Gene: AP3B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3022273
ClinVar RCV Id: RCV003881352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258698.1:p.Gly539Arg
CA3316967
NM_001271769.2:c.1615G>A
CA360187757
NM_001271769.2:c.1615G>C