Canonical Allele Identifier: PA2825448114
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 435517
ClinVar RCV Id: RCV000503966 RCV000765477 RCV001302076 RCV003884579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Asp1247Asn
CA9135155
NM_001079817.3:c.3739G>A