Allele Registry

Canonical Allele Identifier: PA344182

Gene: AIP HGNC NCBI

ClinVar Allele:

49626

ClinVar RCV:

RCV000034103

RCV001237723

RCV004018730

ClinVar Variation:

41204

HGVS (amino-acid)	Matching Registered Transcripts
NP_003968.3:p.Ile257Val	CA344179 NM_003977.4:c.769A>G