Canonical Allele Identifier: PA1139714268
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 859012
ClinVar RCV Id: RCV001065019 RCV002379592
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Lys33Glu
CA6140685
NM_003977.4:c.97A>G