Canonical Allele Identifier: PA915997980
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 825361
ClinVar RCV Id: RCV001023399 RCV003679029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Ala2Pro
CA381545620
NM_003977.4:c.4G>C