Canonical Allele Identifier: PA1139682797
Gene: INS-IGF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 930637
ClinVar RCV Id: RCV001196443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035835.1:p.Thr113Pro
CA379118277
NM_001042376.3:c.337A>C