Canonical Allele Identifier: PA2827251281
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 496406

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Ser11Tyr
CA378380452
NM_001324337.2:c.32C>A