Canonical Allele Identifier: PA2826507224
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2691413
ClinVar RCV Id: RCV003489669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Asn202Ser
CA378386254
NM_001269039.3:c.605A>G