Canonical Allele Identifier: PA2826507114
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 448932
ClinVar RCV Id: RCV000523425 RCV001255488 RCV002367725
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Thr126Ile
CA5689584
NM_001269039.3:c.377C>T