Canonical Allele Identifier: PA2826507091
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1353168
ClinVar RCV Id: RCV001869960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Ser111Cys
CA213256968
NM_001269039.3:c.332C>G