Allele Registry

Canonical Allele Identifier: PA916019374

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000565333

RCV000733154

RCV001554286

RCV003459374

ClinVar Variation:

485053

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289888.1:p.Arg69Cys	CA6140795 NM_001302959.2:c.205C>T