Allele Registry

Canonical Allele Identifier: PA2829477860

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000573085

RCV000765006

RCV001202575

RCV003465251

ClinVar Variation:

485056

HGVS (amino-acid)	Matching Registered Transcripts
NP_003968.3:p.Ala276Val	CA6140987 NM_003977.4:c.827C>T