Canonical Allele Identifier: PA2580187847
Gene: INS HGNC NCBI

Linked Data

ClinVar Variation Id: 1801850
ClinVar RCV Id: RCV002464669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278826.1:p.Pro52Arg
CA5818182
NM_001291897.2:c.155C>G