Allele Registry

Canonical Allele Identifier: PA645505954

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000272200

RCV000567882

RCV001441310

RCV003151020

RCV003967877

ClinVar Variation:

305726

HGVS (amino-acid)	Matching Registered Transcripts
NP_003968.3:p.Val101Met	CA6140781 NM_003977.4:c.301G>A