Canonical Allele Identifier: PA2827250931
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1207211
ClinVar RCV Id: RCV001575126

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Pro16Ser
CA378380651
NM_001324336.2:c.46C>T