Allele Registry

Canonical Allele Identifier: PA2826875517

Gene: AIP HGNC NCBI

ClinVar Allele:

49626

ClinVar RCV:

RCV000034103

RCV001237723

RCV004018730

ClinVar Variation:

41204

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289888.1:p.Ile198Val	CA344179 NM_001302959.2:c.592A>G