Allele Registry

Canonical Allele Identifier: PA2826875501

Gene: AIP HGNC NCBI

ClinVar Allele:

49624

ClinVar RCV:

RCV000034101

ClinVar Variation:

41202

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289888.1:p.Tyr189del	CA344175 NM_001302959.2:c.565_567del