Allele Registry

Canonical Allele Identifier: PA658817381

Gene: AP4B1 HGNC NCBI

ClinVar RCV:

RCV000623523

RCV001849410

RCV002531883

ClinVar Variation:

520727

HGVS (amino-acid)	Matching Registered Transcripts
NP_006585.2:p.Arg206Gln	CA1016061 NM_006594.5:c.617G>A