Canonical Allele Identifier: PA1139672508
Gene: INSR HGNC NCBI

Linked Data

ClinVar Variation Id: 917412
ClinVar RCV Id: RCV001174371
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073285.1:p.Lys487Gln
CA403667101
NM_001079817.3:c.1459A>C