Allele Registry

Canonical Allele Identifier: PA2826875544

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000034105

RCV001027096

RCV001341744

ClinVar Variation:

41206

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289888.1:p.Tyr209Cys	CA344187 NM_001302959.2:c.626A>G