Allele Registry

Canonical Allele Identifier: PA2826875812

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV000034063

RCV000563699

RCV000897518

RCV003894847

ClinVar Variation:

41164

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289889.1:p.Val49Met	CA344063 NM_001302960.2:c.145G>A