Allele Registry

Canonical Allele Identifier: PA2826876230

Gene: AIP HGNC NCBI

ClinVar Allele:

49624

ClinVar RCV:

RCV000034101

ClinVar Variation:

41202

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289889.1:p.Tyr248del	CA344175 NM_001302960.2:c.742_744del