Canonical Allele Identifier: PA2826506937
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 652343
ClinVar RCV Id: RCV000807878 RCV001556226
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Val18Ile
CA378380699
NM_001269039.3:c.52G>A