Allele Registry

Canonical Allele Identifier: PA2826876206

Gene: AIP HGNC NCBI

ClinVar Allele:

49619

ClinVar RCV:

RCV000034096

RCV001379496

RCV004018729

ClinVar Variation:

41197

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289889.1:p.Cys238Tyr	CA344155 NM_001302960.2:c.713G>A