ClinGen Allele Registry
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Canonical Allele Identifier:
PA109191
Gene: INSR
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Transcript change
NP_000199.2:p.Gly58Arg
NM_000208.4:c.172G>A
NM_000208.4:c.172G>C