Canonical Allele Identifier: PA1139672479
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 987803
ClinVar RCV Id: RCV001269129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Asn384Ser
CA403667796
NM_001079817.3:c.1151A>G