Allele Registry

Canonical Allele Identifier: PA2826875389

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000034088

RCV001024601

RCV001326206

ClinVar Variation:

41189

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289888.1:p.Val136Ala	CA344130 NM_001302959.2:c.407T>C