Canonical Allele Identifier: PA2826875800
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2102813
ClinVar RCV Id: RCV003028710
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Asp45Glu
CA6140734
NM_001302960.2:c.135C>A
CA381546511
NM_001302960.2:c.135C>G