Canonical Allele Identifier: PA2825448147
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 1337699
ClinVar RCV Id: RCV001820713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Met1307Ile
CA9135113
NM_001079817.3:c.3921G>C
CA9135114
NM_001079817.3:c.3921G>A
CA403668610
NM_001079817.3:c.3921G>T