Canonical Allele Identifier: PA2580300201
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_003968.3:p.Tyr268His
CA381554362
NM_003977.4:c.802T>C