Canonical Allele Identifier: PA2826875742
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 826838
ClinVar RCV Id: RCV001026039 RCV001305281 RCV003461414
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Glu24Gln
CA224160955
NM_001302960.2:c.70G>C