Allele Registry

Canonical Allele Identifier: PA2826875567

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000034111

RCV001366847

ClinVar Variation:

41212

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289888.1:p.Ala218Pro	CA344205 NM_001302959.2:c.652G>C