Canonical Allele Identifier: PA2826875960
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 843599
ClinVar RCV Id: RCV001046267 RCV002451181
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Arg119Gln
CA6140790
NM_001302960.2:c.356G>A