Allele Registry

Canonical Allele Identifier: PA645387800

Gene: AP4M1 HGNC NCBI

ClinVar Variation Id: 386755

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