Canonical Allele Identifier: PA2573195589
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1632842
ClinVar RCV Id: RCV002119323
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Gly281Ser
CA475509521
NM_001302960.2:c.841G>A