Canonical Allele Identifier: PA916019385
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 822562

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Gly283Arg
CA381554882
NM_001302960.2:c.847G>C