Allele Registry

Canonical Allele Identifier: PA2826875838

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000034065

RCV001012978

RCV001038333

RCV001879696

ClinVar Variation:

41166

1375499

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289889.1:p.Lys58Asn	CA344071 NM_001302960.2:c.174G>C CA6140746 NM_001302960.2:c.174G>T