Canonical Allele Identifier: PA658671319
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 448932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Thr126Ile
CA5689584
NM_007373.4:c.377C>T