Canonical Allele Identifier: PA2826875972
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 3223612
ClinVar RCV Id: RCV004516376
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Gln126Arg
CA381549417
NM_001302960.2:c.377A>G