Canonical Allele Identifier: PA658723044
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 496406

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Ser11Tyr
CA378380452
NM_007373.4:c.32C>A