Canonical Allele Identifier: PA2826506992
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2200060
ClinVar RCV Id: RCV002644031
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Glu42Asp
CA378381637
NM_001269039.3:c.126A>C
CA378381638
NM_001269039.3:c.126A>T