Canonical Allele Identifier: PA2826875228
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 821051
ClinVar RCV Id: RCV001015103 RCV001323868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Val18Met
CA6140754
NM_001302959.2:c.52G>A