Canonical Allele Identifier: PA124216
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 14681
ClinVar RCV Id: RCV000015795
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Gly393Arg
CA124215
NM_001079817.3:c.1177G>A
CA403667742
NM_001079817.3:c.1177G>C