Canonical Allele Identifier: PA124256
Gene: INSR HGNC NCBI
ClinVar RCV:
RCV000015818
ClinVar Variation:
14703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Arg113Pro
CA124255
NM_001079817.3:c.338G>C