Allele Registry

Canonical Allele Identifier: PA2826875832

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV001102833

RCV001326205

RCV002402499

ClinVar Variation:

877266

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289889.1:p.Arg56Cys	CA6140744 NM_001302960.2:c.166C>T