Allele Registry

Canonical Allele Identifier: PA916019373

Gene: AIP HGNC NCBI

ClinVar Allele:

49598

ClinVar RCV:

RCV000034075

RCV001021265

RCV001052633

ClinVar Variation:

41176

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289888.1:p.Arg69His	CA344099 NM_001302959.2:c.206G>A