Canonical Allele Identifier: PA2826875588
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1764237
ClinVar RCV Id: RCV002449666
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Ala230Val
CA381554985
NM_001302959.2:c.689C>T