Allele Registry

Canonical Allele Identifier: PA2829591764

Gene: AP1M2 HGNC NCBI

ClinVar RCV:

RCV004170028

ClinVar Variation:

2328111

HGVS (amino-acid)	Matching Registered Transcripts
NP_005489.2:p.Ser331Thr	CA9197755 NM_005498.5:c.992G>C