Canonical Allele Identifier: PA2826875745
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 954536
ClinVar RCV Id: RCV001227005 RCV002255634 RCV003469398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Leu25Phe
CA6140676
NM_001302960.2:c.73C>T