Allele Registry

Canonical Allele Identifier: PA658820141

Gene: AP4M1 HGNC NCBI

ClinVar Allele:

513289

ClinVar RCV:

RCV000625788

ClinVar Variation:

522649

HGVS (amino-acid)	Matching Registered Transcripts
NP_004713.2:p.Phe409Leu	CA4375034 NM_004722.4:c.1225T>C CA368476862 NM_004722.4:c.1227C>A CA368476878 NM_004722.4:c.1227C>G