Canonical Allele Identifier: PA2825448129
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 593002
ClinVar RCV Id: RCV000727925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Asn1276Ser
CA9135128
NM_001079817.3:c.3827A>G