Allele Registry

Canonical Allele Identifier: PA2826875661

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000564964

RCV001040402

RCV001526825

ClinVar Variation:

485063

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289888.1:p.Arg264Trp	CA6141013 NM_001302959.2:c.790C>T