Allele Registry

Canonical Allele Identifier: PA2826875738

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000005167

ClinVar Variation:

4889

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289889.1:p.Gly23_Glu24del	CA340302 NM_001302960.2:c.66_71del