Canonical Allele Identifier: PA2826875769
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1767515
ClinVar RCV Id: RCV002374349 RCV003565546
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Thr32Asn
CA381545891
NM_001302960.2:c.95C>A