Canonical Allele Identifier: PA2825448135
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2231216
ClinVar RCV Id: RCV002707940
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Pro1284Ser
CA403668775
NM_001079817.3:c.3850C>T