Canonical Allele Identifier: PA2826875818
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2010264
ClinVar RCV Id: RCV002850986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Asp51Gly
CA381546623
NM_001302960.2:c.152A>G