Canonical Allele Identifier: PA2827251280
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1914478
ClinVar RCV Id: RCV002612750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Asp10Tyr
CA378380385
NM_001324337.2:c.28G>T