Canonical Allele Identifier: PA2827251006
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1310782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Ile114Met
CA378384376
NM_001324336.2:c.342A>G