Canonical Allele Identifier: PA2580187820
Gene: INS HGNC NCBI

Linked Data

ClinVar Variation Id: 2311109
ClinVar RCV Id: RCV004158356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278826.1:p.Gly18Arg
CA5818198
NM_001291897.2:c.52G>C
CA379122156
NM_001291897.2:c.52G>A