Canonical Allele Identifier: PA2573061798
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 1337699
ClinVar RCV Id: RCV001820713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000199.2:p.Met1319Ile
CA9135113
NM_000208.4:c.3957G>C
CA9135114
NM_000208.4:c.3957G>A
CA403668610
NM_000208.4:c.3957G>T