Canonical Allele Identifier: PA2741829847
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 3061041
ClinVar RCV Id: RCV004542613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Glu418Asp
CA403667589
NM_001079817.3:c.1254G>T
CA403667590
NM_001079817.3:c.1254G>C