Allele Registry

Canonical Allele Identifier: PA2826875488

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000034099

RCV001366846

RCV002371817

ClinVar Variation:

41200

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289888.1:p.Lys182Glu	CA344167 NM_001302959.2:c.544A>G