Canonical Allele Identifier: PA2826875616
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 4893
ClinVar RCV Id: RCV000005171 RCV000439236 RCV000508590 RCV000571906 RCV000766368 RCV000735427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Arg245Gln
CA340308
NM_001302959.2:c.734G>A