Canonical Allele Identifier: PA2826875726
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1369274
ClinVar RCV Id: RCV001894859 RCV002343929
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Gln19Arg
CA381545811
NM_001302960.2:c.56A>G