Canonical Allele Identifier: PA2826876076
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2675313

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Lys175Gln
CA381550580
NM_001302960.2:c.523A>C