Canonical Allele Identifier: PA1139714242
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 954484
ClinVar RCV Id: RCV001226942 RCV002375227
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Asp30Tyr
CA381545876
NM_003977.4:c.88G>T