Canonical Allele Identifier: PA205600
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 211190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Ser748Leu
CA205599
NM_000208.4:c.2243C>T