Canonical Allele Identifier: PA2826875837
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1376671
ClinVar RCV Id: RCV001886062
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Gly57Asp
CA381546733
NM_001302960.2:c.170G>A