Canonical Allele Identifier: PA2499247196
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1058143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Gln261Arg
CA381554279
NM_001302960.2:c.782A>G