Canonical Allele Identifier: PA2573258004
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1502464
ClinVar RCV Id: RCV002010992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Lys169Arg
CA378385738
NM_007373.4:c.506A>G