Canonical Allele Identifier: PA2826875722
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 41184
ClinVar RCV Id: RCV000034083 RCV000560928 RCV000893230 RCV001554284 RCV003924890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Arg16His
CA344116
NM_001302960.2:c.47G>A