Allele Registry

Canonical Allele Identifier: PA2826875616

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000005171

RCV000439236

RCV000508590

RCV000571906

RCV000735427

RCV000766368

ClinVar Variation:

4893

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289888.1:p.Arg245Gln	CA340308 NM_001302959.2:c.734G>A