Canonical Allele Identifier: PA124228
Gene: INSR HGNC NCBI
ClinVar RCV:
RCV000015804
ClinVar Variation:
14689
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Leu260Pro
CA124227
NM_001079817.3:c.779T>C