Allele Registry

Canonical Allele Identifier: PA658678512

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000564964

RCV001040402

RCV001526825

ClinVar Variation:

485063

HGVS (amino-acid)	Matching Registered Transcripts
NP_003968.3:p.Arg323Trp	CA6141013 NM_003977.4:c.967C>T