Canonical Allele Identifier: PA2826875234
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1790270
ClinVar RCV Id: RCV002450164 RCV003730217
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Thr20Ile
CA381547170
NM_001302959.2:c.59C>T