Allele Registry

Canonical Allele Identifier: PA2826875834

Gene: AIP HGNC NCBI

ClinVar Allele:

49587

ClinVar RCV:

RCV000034064

ClinVar Variation:

41165

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289889.1:p.Arg56Ser	CA344067 NM_001302960.2:c.166C>A