Canonical Allele Identifier: PA2827250935
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 877714
ClinVar RCV Id: RCV001103683

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Pro19Arg
CA378380782
NM_001324336.2:c.56C>G