Canonical Allele Identifier: PA2826875590
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 839402
ClinVar RCV Id: RCV001041150 RCV002445231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Leu233Val
CA6140994
NM_001302959.2:c.697C>G