Canonical Allele Identifier: PA2826506903
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2265459
ClinVar RCV Id: RCV004120669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Ser2Thr
CA378380117
NM_001269039.3:c.5G>C