Canonical Allele Identifier: PA108748
Gene: INS HGNC NCBI

Linked Data

ClinVar Variation Id: 21114
ClinVar RCV Id: RCV000020204 RCV000030069 RCV001089452 RCV003445080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000198.1:p.Cys43Gly
CA214063
NM_000207.3:c.127T>G