Canonical Allele Identifier: PA2829477878
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1063288
ClinVar RCV Id: RCV001373112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Ala284Thr
CA381554828
NM_003977.4:c.850G>A