Canonical Allele Identifier: PA2826506925
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 496406

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Ser11Tyr
CA378380452
NM_001269039.3:c.32C>A