Allele Registry

Canonical Allele Identifier: PA2826875808

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000034062

RCV001852688

ClinVar Variation:

41163

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289889.1:p.Gly47_Arg54del	CA344059 NM_001302960.2:c.140_163del