Canonical Allele Identifier: PA2826875764
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 954484
ClinVar RCV Id: RCV001226942 RCV002375227
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Asp30Tyr
CA381545876
NM_001302960.2:c.88G>T