Canonical Allele Identifier: PA2826876067
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2447163
ClinVar RCV Id: RCV003165087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Thr171Arg
CA381550513
NM_001302960.2:c.512C>G