Allele Registry

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Canonical Allele Identifier: PA2826875309

Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 3223615

ClinVar RCV Id: RCV004516379

ClinVar Variation Id: 3223616

ClinVar RCV Id: RCV004516380

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289888.1:p.Val98Leu	CA381550224 NM_001302959.2:c.292G>T CA381550226 NM_001302959.2:c.292G>C