Allele Registry

SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-09-25T08:00:00-0500
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Canonical Allele Identifier: PA2826875838

Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 41166

ClinVar RCV Id: RCV000034065 RCV001012978 RCV001038333

ClinVar Variation Id: 1375499

ClinVar RCV Id: RCV001879696

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289889.1:p.Lys58Asn	CA344071 NM_001302960.2:c.174G>C CA6140746 NM_001302960.2:c.174G>T