Allele Registry

Canonical Allele Identifier: PA2580190288

Gene: AP1M2 HGNC NCBI

ClinVar RCV:

RCV004170028

ClinVar Variation:

2328111

HGVS (amino-acid)	Matching Registered Transcripts
NP_001287816.1:p.Ser333Thr	CA9197755 NM_001300887.2:c.998G>C