Allele Registry

Canonical Allele Identifier: PA3057550442

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000034107

RCV001027111

RCV001386204

ClinVar Variation:

41208

HGVS (amino-acid)	Matching Registered Transcripts
NP_003968.3:p.Phe269_His275dup	CA344192 NM_003977.4:c.805_825dup