Canonical Allele Identifier: PA2826875773
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 859012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Lys33Glu
CA6140685
NM_001302960.2:c.97A>G