Allele Registry

Canonical Allele Identifier: PA916043908

Gene: AP4M1 HGNC NCBI

ClinVar RCV:

RCV000549259

RCV001849402

ClinVar Variation:

471069

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350600.1:p.Tyr291Ser	CA368472432 NM_001363671.2:c.872A>C