Canonical Allele Identifier: PA2826875716
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 824668
ClinVar RCV Id: RCV001022033 RCV001063933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Gln14Pro
CA381545778
NM_001302960.2:c.41A>C