Canonical Allele Identifier: PA1139688399
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 843599
ClinVar RCV Id: RCV001046267 RCV002451181
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Arg60Gln
CA6140790
NM_001302959.2:c.179G>A