Canonical Allele Identifier: PA2826875714
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1486213
ClinVar RCV Id: RCV002003430 RCV002361353
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Ile13Val
CA381545771
NM_001302960.2:c.37A>G