Canonical Allele Identifier: PA2827250916
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 6821

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Ser2Gly
CA118524
NM_001324336.2:c.4A>G