Canonical Allele Identifier: PA2826507095
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 372672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Ile112Thr
CA5689578
NM_001269039.3:c.335T>C