Canonical Allele Identifier: PA2573258005
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1413835
ClinVar RCV Id: RCV001928346

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Leu171Met
CA378385762
NM_007373.4:c.511C>A