Canonical Allele Identifier: PA205600
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 211190
ClinVar RCV Id: RCV000192643 RCV000306720 RCV000363783 RCV000391048 RCV000664156 RCV000725945 RCV002517086 RCV004530120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Ser748Leu
CA205599
NM_000208.4:c.2243C>T