Canonical Allele Identifier: PA645501323
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 434226
ClinVar RCV Id: RCV000501595
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006585.2:p.Pro280Ser
CA1015999
NM_006594.5:c.838C>T