Canonical Allele Identifier: PA2580192321
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1742591
ClinVar RCV Id: RCV002335341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Val98Glu
CA381550229
NM_001302959.2:c.293T>A