Canonical Allele Identifier: PA2826875579
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1063288
ClinVar RCV Id: RCV001373112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Ala225Thr
CA381554828
NM_001302959.2:c.673G>A