Canonical Allele Identifier: PA2580300206
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1764237
ClinVar RCV Id: RCV002449666
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Ala289Val
CA381554985
NM_003977.4:c.866C>T