Canonical Allele Identifier: PA2826507011
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1508675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Ser57Pro
CA5689559
NM_001269039.3:c.169T>C