Allele Registry

Canonical Allele Identifier: PA916043923

Gene: AP4M1 HGNC NCBI

ClinVar Allele:

513289

ClinVar RCV:

RCV000625788

ClinVar Variation:

522649

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350600.1:p.Phe416Leu	CA4375034 NM_001363671.2:c.1246T>C CA368476862 NM_001363671.2:c.1248C>A CA368476878 NM_001363671.2:c.1248C>G