Allele Registry

Canonical Allele Identifier: PA2826875563

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000573085

RCV000765006

RCV001202575

RCV003465251

ClinVar Variation:

485056

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289888.1:p.Ala217Val	CA6140987 NM_001302959.2:c.650C>T