Allele Registry

Canonical Allele Identifier: PA658678441

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000561910

RCV000765005

RCV001054806

RCV001764674

ClinVar Variation:

485052

HGVS (amino-acid)	Matching Registered Transcripts
NP_003968.3:p.Arg9Gln	CA6140668 NM_003977.4:c.26G>A