Canonical Allele Identifier: PA2826155695
Gene: INS HGNC NCBI

Linked Data

ClinVar Variation Id: 13391
ClinVar RCV Id: RCV000014323 RCV001851851 RCV003445068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172027.1:p.Arg46Gln
CA123086
NM_001185098.2:c.137G>A