Allele Registry

Canonical Allele Identifier: PA2826876096

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV002575760

ClinVar Variation:

1896473

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289889.1:p.Gln184Lys	CA6140867 NM_001302960.2:c.550C>A