Canonical Allele Identifier: PA2826875316
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 962699
ClinVar RCV Id: RCV001236604 RCV002339652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Pro101Thr
CA381550280
NM_001302959.2:c.301C>A