Canonical Allele Identifier: PA2826875397
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1041400
ClinVar RCV Id: RCV001345200
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Ala140Pro
CA381551054
NM_001302959.2:c.418G>C