Canonical Allele Identifier: PA2827251334
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1014118
ClinVar RCV Id: RCV001312811 RCV003135959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Ala78Val
CA5689564
NM_001324337.2:c.233C>T