Canonical Allele Identifier: PA645501321
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 408760
ClinVar RCV Id: RCV000475749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006585.2:p.Ala263Thr
CA1016014
NM_006594.5:c.787G>A