Canonical Allele Identifier: PA2827251388
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1502464
ClinVar RCV Id: RCV002010992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Lys169Arg
CA378385738
NM_001324337.2:c.506A>G