Canonical Allele Identifier: PA2825448020
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 631539
ClinVar RCV Id: RCV000778147 RCV001132182 RCV001132181 RCV002487597
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Gly1036Asp
CA9135351
NM_001079817.3:c.3107G>A