Canonical Allele Identifier: PA2741935641
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3016298
ClinVar RCV Id: RCV003876449

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Leu107Phe
CA378384038
NM_007373.4:c.321A>C
CA378384042
NM_007373.4:c.321A>T