Canonical Allele Identifier: PA2826876118
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 41189
ClinVar RCV Id: RCV000034088 RCV001024601 RCV001326206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Val195Ala
CA344130
NM_001302960.2:c.584T>C