Canonical Allele Identifier: PA645455639
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 372672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Ile112Thr
CA5689578
NM_007373.4:c.335T>C