Canonical Allele Identifier: PA2827251057
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2691413
ClinVar RCV Id: RCV003489669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Asn202Ser
CA378386254
NM_001324336.2:c.605A>G