Canonical Allele Identifier: PA2827251378
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 452915
ClinVar RCV Id: RCV000523780 RCV001853695 RCV004023626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Met149Val
CA5689591
NM_001324337.2:c.445A>G