Canonical Allele Identifier: PA2826506918
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1914478
ClinVar RCV Id: RCV002612750

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Asp10Tyr
CA378380385
NM_001269039.3:c.28G>T