Allele Registry

Canonical Allele Identifier: PA2826875888

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000034069

ClinVar Variation:

41170

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289889.1:p.Glu84Lys	CA344084 NM_001302960.2:c.250G>A