Allele Registry

Canonical Allele Identifier: PA645501319

Gene: AP4B1 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

364370

ClinVar RCV:

RCV000425918

RCV000463656

RCV001251671

RCV001821192

RCV001848780

RCV002313102

RCV003912733

ClinVar Variation:

386852

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_006585.2:p.Val252Ala	CA1016017 NM_006594.5:c.755T>C