Canonical Allele Identifier: PA2826875833
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1777879
ClinVar RCV Id: RCV002406010 RCV003100788
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Arg56Pro
CA381546718
NM_001302960.2:c.167G>C