Canonical Allele Identifier: PA2826875872
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 387905
ClinVar RCV Id: RCV000433700 RCV001014992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Ile76Val
CA16606298
NM_001302960.2:c.226A>G