Canonical Allele Identifier: PA2499265285
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1026055
ClinVar RCV Id: RCV001326457 RCV002464041
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Asp263del
CA6140934
NM_003977.4:c.785_787del