Canonical Allele Identifier: PA2826155627
Gene: INS HGNC NCBI

Linked Data

ClinVar Variation Id: 68728
ClinVar RCV Id: RCV000059610 RCV003445478 RCV003925020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172026.1:p.Leu68Met
CA219842
NM_001185097.2:c.202C>A