Canonical Allele Identifier: PA2825448047
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2494664
ClinVar RCV Id: RCV003206600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Ser1052Asn
CA304873334
NM_001079817.3:c.3155G>A