Canonical Allele Identifier: PA2826875359
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1429255
ClinVar RCV Id: RCV001938839 RCV002344070
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Leu122Arg
CA381550703
NM_001302959.2:c.365T>G