Allele Registry

Canonical Allele Identifier: PA2826875605

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000034113

RCV000571818

RCV001357152

RCV003904890

ClinVar Variation:

41214

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289888.1:p.Ala240Val	CA344210 NM_001302959.2:c.719C>T