Allele Registry

Canonical Allele Identifier: PA645387800

Gene: AP4M1 HGNC NCBI

ClinVar RCV:

RCV000434728

RCV001088095

RCV003959945

ClinVar Variation:

386755

HGVS (amino-acid)	Matching Registered Transcripts
NP_004713.2:p.Glu99Lys	CA4374557 NM_004722.4:c.295G>A