Canonical Allele Identifier: PA2826506952
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2446233
ClinVar RCV Id: RCV003156587

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Glu25Gln
CA378380960
NM_001269039.3:c.73G>C