Allele Registry

Canonical Allele Identifier: PA2826876260

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV001027105

RCV003718310

ClinVar Variation:

827413

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289889.1:p.Leu266Phe	CA475509423 NM_001302960.2:c.796C>T