Allele Registry

Canonical Allele Identifier: PA2826876118

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000034088

RCV001024601

RCV001326206

ClinVar Variation:

41189

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289889.1:p.Val195Ala	CA344130 NM_001302960.2:c.584T>C