Canonical Allele Identifier: PA2826876045
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 962699
ClinVar RCV Id: RCV001236604 RCV002339652
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Pro160Thr
CA381550280
NM_001302960.2:c.478C>A