ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA916018274
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_001278826.1:p.Gly90Cys
CA341645
NM_001291897.2:c.268G>T