Canonical Allele Identifier: PA1139736041
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 877714
ClinVar RCV Id: RCV001103683
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Pro19Arg
CA378380782
NM_007373.4:c.56C>G