Canonical Allele Identifier: PA2826876113
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1449487
ClinVar RCV Id: RCV002014527 RCV004043923
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Glu192Gly
CA6140875
NM_001302960.2:c.575A>G