Canonical Allele Identifier: PA2826875713
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1406802
ClinVar RCV Id: RCV001906995 RCV002359402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Ile13Asn
CA6140671
NM_001302960.2:c.38T>A