Canonical Allele Identifier: PA2580300107
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1780355
ClinVar RCV Id: RCV002407870
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Ala6Glu
CA381545699
NM_003977.4:c.17C>A