Canonical Allele Identifier: PA2826876101
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2586853
ClinVar RCV Id: RCV003358430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Gly186Asp
CA381550811
NM_001302960.2:c.557G>A