Allele Registry

Canonical Allele Identifier: PA2826875242

Gene: AIP HGNC NCBI

ClinVar Allele:

49592

ClinVar RCV:

RCV000034069

ClinVar Variation:

41170

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289888.1:p.Glu25Lys	CA344084 NM_001302959.2:c.73G>A