Allele Registry

Canonical Allele Identifier: PA2828102349

Gene: AP4M1 HGNC NCBI

ClinVar Variation Id: 386755

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350600.1:p.Glu106Lys	CA4374557 NM_001363671.2:c.316G>A