Canonical Allele Identifier: PA2827251003
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 372672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Ile112Thr
CA5689578
NM_001324336.2:c.335T>C