Allele Registry

Canonical Allele Identifier: PA2826875978

Gene: AIP HGNC NCBI

ClinVar Allele:

49598

ClinVar RCV:

RCV000034075

RCV001021265

RCV001052633

ClinVar Variation:

41176

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289889.1:p.Arg128His	CA344099 NM_001302960.2:c.383G>A