Canonical Allele Identifier: PA2826876092
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 999844
ClinVar RCV Id: RCV001295893 RCV002350518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Ile182Thr
CA381550715
NM_001302960.2:c.545T>C