Canonical Allele Identifier: PA117129
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 4892
ClinVar RCV Id: RCV000034106 RCV000005170 RCV003555922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Leu266Ile
CA117126
NM_001302960.2:c.796C>A