Canonical Allele Identifier: PA2826875844
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1005479
ClinVar RCV Id: RCV001302360 RCV002411962
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Glu61Gly
CA381546832
NM_001302960.2:c.182A>G