Canonical Allele Identifier: PA915998224
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 822637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Ala289Thr
CA381554966
NM_003977.4:c.865G>A