Allele Registry

Canonical Allele Identifier: PA2826875922

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000272200

RCV000567882

RCV001441310

RCV003151020

RCV003967877

ClinVar Variation:

305726

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289889.1:p.Val101Met	CA6140781 NM_001302960.2:c.301G>A