Allele Registry

Canonical Allele Identifier: PA2826875828

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV001322598

RCV003284193

RCV003469552

ClinVar Variation:

1022659

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289889.1:p.Ala55Val	CA381546698 NM_001302960.2:c.164C>T