Canonical Allele Identifier: PA2826875647
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 823287
ClinVar RCV Id: RCV001019413 RCV001212933 RCV001543119 RCV002254716
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Asp258Tyr
CA224166060
NM_001302959.2:c.772G>T