Allele Registry

Canonical Allele Identifier: PA124268

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015824

RCV001851881

ClinVar Variation:

14709

HGVS (amino-acid)	Matching Registered Transcripts
NP_000199.2:p.Met1180Ile	CA124266 NM_000208.4:c.3540G>A CA403669576 NM_000208.4:c.3540G>T CA403669577 NM_000208.4:c.3540G>C