Canonical Allele Identifier: PA2826875922
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 305726
ClinVar RCV Id: RCV000272200 RCV000567882 RCV001441310 RCV003151020 RCV003967877
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Val101Met
CA6140781
NM_001302960.2:c.301G>A