Canonical Allele Identifier: PA2580369045
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1734179
ClinVar RCV Id: RCV002353033
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Gln124Lys
CA378384666
NM_007373.4:c.370C>A