Canonical Allele Identifier: PA2826507233
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 948626
ClinVar RCV Id: RCV001219923 RCV002484194 RCV004032377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Val207Met
CA213257079
NM_001269039.3:c.619G>A