Allele Registry

Canonical Allele Identifier: PA2826876259

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000034107

RCV001027111

RCV001386204

ClinVar Variation:

41208

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289889.1:p.Leu266_Pro272dup	CA344192 NM_001302960.2:c.797_817dup