Canonical Allele Identifier: PA1139697739
Gene: INS HGNC NCBI

Linked Data

ClinVar Variation Id: 931331
ClinVar RCV Id: RCV001197790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278826.1:p.Pro52Leu
CA379121407
NM_001291897.2:c.155C>T