Canonical Allele Identifier: PA2573257988
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1514651
ClinVar RCV Id: RCV002048309

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Gly35Trp
CA378381372
NM_007373.4:c.103G>T