Canonical Allele Identifier: PA2573257999
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1353168
ClinVar RCV Id: RCV001869960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Ser111Cys
CA213256968
NM_007373.4:c.332C>G