Canonical Allele Identifier: PA2826875686
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1750985
ClinVar RCV Id: RCV002357972
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Ala2Gly
CA381545625
NM_001302960.2:c.5C>G