Canonical Allele Identifier: PA915964974
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 289211
ClinVar RCV Id: RCV000365243 RCV000308234 RCV000726299 RCV000408260 RCV000664158 RCV002518075 RCV003884445
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Leu14Pro
CA9136191
NM_001079817.3:c.41T>C