Canonical Allele Identifier: PA645402458
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 435516
ClinVar RCV Id: RCV000502540 RCV001857113 RCV002476006
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Ile1137Thr
CA9135252
NM_000208.4:c.3410T>C