Canonical Allele Identifier: PA1139714411
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 864210
ClinVar RCV Id: RCV001071341 RCV002436690
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Lys93Arg
CA224163282
NM_003977.4:c.278A>G