Canonical Allele Identifier: PA109022
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 1685300
ClinVar RCV Id: RCV002249027 RCV003094009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Arg1378Gln
CA9135084
NM_000208.4:c.4133G>A