Allele Registry

Canonical Allele Identifier: PA916043929

Gene: AP4M1 HGNC NCBI

ClinVar RCV:

RCV000192888

RCV000860999

RCV001507706

RCV001847852

RCV003895240

ClinVar Variation:

210207

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350600.1:p.Ala455Thr	CA206016 NM_001363671.2:c.1363G>A