Canonical Allele Identifier: PA2573176959
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 1500944
ClinVar RCV Id: RCV002016037
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Gly386Ser
CA9135898
NM_001079817.3:c.1156G>A