Allele Registry

Canonical Allele Identifier: PA344218

Gene: AIP HGNC NCBI

ClinVar Allele:

49638

ClinVar RCV:

RCV000034115

RCV001061414

RCV002371818

ClinVar Variation:

41216

HGVS (amino-acid)	Matching Registered Transcripts
NP_003968.3:p.Ala322Val	CA344215 NM_003977.4:c.965C>T