Canonical Allele Identifier: PA124267
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 14709

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Met1168Ile
CA124266
NM_001079817.3:c.3504G>A
CA403669576
NM_001079817.3:c.3504G>T
CA403669577
NM_001079817.3:c.3504G>C