Allele Registry

Canonical Allele Identifier: PA2826363051

Gene: AP4B1 HGNC NCBI

ClinVar RCV:

RCV000145016

RCV000986397

RCV001847774

RCV002312627

ClinVar Variation:

157718

HGVS (amino-acid)	Matching Registered Transcripts
NP_001240782.1:p.Leu381Ser	CA171108 NM_001253853.3:c.1142T>C