Canonical Allele Identifier: PA2826507156
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1502464
ClinVar RCV Id: RCV002010992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Lys169Arg
CA378385738
NM_001269039.3:c.506A>G