Canonical Allele Identifier: PA2825448142
Gene: INSR HGNC NCBI
ClinVar RCV:
RCV002001226
ClinVar Variation:
1486096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Glu1301Lys
CA9135116
NM_001079817.3:c.3901G>A