Canonical Allele Identifier: PA2826875543
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2452492
ClinVar RCV Id: RCV003172586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Tyr209His
CA381554362
NM_001302959.2:c.625T>C