Canonical Allele Identifier: PA2826875691
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2094440
ClinVar RCV Id: RCV003010287
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Ile4Thr
CA381545667
NM_001302960.2:c.11T>C