Canonical Allele Identifier: PA2826155641
Gene: INS HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172026.1:p.Val92Leu
CA123080
NM_001185097.2:c.274G>T
CA379120889
NM_001185097.2:c.274G>C