Canonical Allele Identifier: PA108806
Gene: INS HGNC NCBI

Linked Data

ClinVar Variation Id: 21118
ClinVar RCV Id: RCV000020208 RCV003460486
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000198.1:p.Gly90Cys
CA341645
NM_000207.3:c.268G>T