Canonical Allele Identifier: PA344218
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 41216
ClinVar RCV Id: RCV000034115 RCV001061414 RCV002371818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Ala322Val
CA344215
NM_003977.4:c.965C>T