Canonical Allele Identifier: PA2826875900
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1795400
ClinVar RCV Id: RCV002437585
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Asp91Glu
CA381547415
NM_001302960.2:c.273C>A
CA381547418
NM_001302960.2:c.273C>G