Canonical Allele Identifier: PA2829671068
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1028532
ClinVar RCV Id: RCV001329593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006585.2:p.Arg224His
CA28997545
NM_006594.5:c.671G>A