ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825084436
Gene: INS
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1801850
ClinVar RCV Id:
RCV002464669
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000198.1:p.Pro52Arg
CA5818182
NM_000207.3:c.155C>G