Allele Registry

Canonical Allele Identifier: PA1139714310

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV001102833

RCV001326205

RCV002402499

ClinVar Variation:

877266

HGVS (amino-acid)	Matching Registered Transcripts
NP_003968.3:p.Arg56Cys	CA6140744 NM_003977.4:c.166C>T