Allele Registry

Canonical Allele Identifier: PA2826875657

Gene: AIP HGNC NCBI

ClinVar Allele:

49638

ClinVar RCV:

RCV000034115

RCV001061414

RCV002371818

ClinVar Variation:

41216

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289888.1:p.Ala263Val	CA344215 NM_001302959.2:c.788C>T