Canonical Allele Identifier: PA2826876128
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1020160
ClinVar RCV Id: RCV001319695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Lys201Arg
CA381551112
NM_001302960.2:c.602A>G