Canonical Allele Identifier: PA1139714376
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 859123
ClinVar RCV Id: RCV001065160 RCV002411587
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Pro59Ser
CA381546783
NM_003977.4:c.175C>T