Canonical Allele Identifier: PA2826875364
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1747590
ClinVar RCV Id: RCV002349642
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Ile123Val
CA381550706
NM_001302959.2:c.367A>G