Canonical Allele Identifier: PA2827251284
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Glu13Ala
CA297169
NM_001324337.2:c.38A>C