Allele Registry

Canonical Allele Identifier: PA2826875926

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000034073

RCV001018537

RCV001214294

ClinVar Variation:

41174

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289889.1:p.Lys103Arg	CA344094 NM_001302960.2:c.308A>G