Canonical Allele Identifier: PA2826506908
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2640834
ClinVar RCV Id: RCV003422881

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Ser4Asn
CA378380168
NM_001269039.3:c.11G>A