Canonical Allele Identifier: PA206181
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 211200
ClinVar RCV Id: RCV000192986 RCV000725826 RCV004530122
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Thr320Met
CA206180
NM_000208.4:c.959C>T