Canonical Allele Identifier: PA2826155721
Gene: INS HGNC NCBI

Linked Data

ClinVar Variation Id: 21118
ClinVar RCV Id: RCV000020208 RCV003460486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172027.1:p.Gly90Cys
CA341645
NM_001185098.2:c.268G>T