Canonical Allele Identifier: PA2826876129
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1751105
ClinVar RCV Id: RCV002358092
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Lys201Gln
CA381551102
NM_001302960.2:c.601A>C