Canonical Allele Identifier: PA208960
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 211195
ClinVar RCV Id: RCV000194649 RCV000286740 RCV000341695 RCV000445398 RCV000382385 RCV000725784 RCV004530121
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Asp946Glu
CA208959
NM_000208.4:c.2838C>G
CA403671905
NM_000208.4:c.2838C>A