Canonical Allele Identifier: PA2826507057
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 981609
ClinVar RCV Id: RCV001261150 RCV001293615
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Met103Val
CA5689574
NM_001269039.3:c.307A>G