Canonical Allele Identifier: PA1139697757
Gene: INS HGNC NCBI

Linked Data

ClinVar Variation Id: 435510
ClinVar RCV Id: RCV000499487 RCV002464227
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278826.1:p.Tyr108del
CA645372891
NM_001291897.2:c.323_325del