Canonical Allele Identifier: PA124270
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 14710
ClinVar RCV Id: RCV000015825
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Trp439Ser
CA124269
NM_001079817.3:c.1316G>C