Canonical Allele Identifier: PA2573089800
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1310782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Ile114Met
CA378384376
NM_007373.4:c.342A>G