Canonical Allele Identifier: PA2826155706
Gene: INS HGNC NCBI

Linked Data

ClinVar Variation Id: 1678636
ClinVar RCV Id: RCV002225237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172027.1:p.Pro52His
CA379121410
NM_001185098.2:c.155C>A