Canonical Allele Identifier: PA2826875749
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2873002
ClinVar RCV Id: RCV003709622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Pro26Ala
CA381545849
NM_001302960.2:c.76C>G