Allele Registry

Canonical Allele Identifier: PA351376

Gene: AP4E1 HGNC NCBI

ClinVar RCV:

RCV002518399

ClinVar Variation:

242436

HGVS (amino-acid)	Matching Registered Transcripts
NP_031373.2:p.Glu801Lys	CA351375 NM_007347.5:c.2401G>A