Canonical Allele Identifier: PA2826155723
Gene: INS HGNC NCBI

Linked Data

ClinVar Variation Id: 13381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172027.1:p.Val92Leu
CA123080
NM_001185098.2:c.274G>T
CA379120889
NM_001185098.2:c.274G>C