Allele Registry

Canonical Allele Identifier: PA344097

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000034073

RCV001018537

RCV001214294

ClinVar Variation:

41174

HGVS (amino-acid)	Matching Registered Transcripts
NP_003968.3:p.Lys103Arg	CA344094 NM_003977.4:c.308A>G