Canonical Allele Identifier: PA915964979
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 14699
ClinVar RCV Id: RCV000015814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Gly58Arg
CA124247
NM_001079817.3:c.172G>A
CA403160518
NM_001079817.3:c.172G>C