Canonical Allele Identifier: PA2826507182
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 996269
ClinVar RCV Id: RCV001290609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Ser186Ala
CA378386010
NM_001269039.3:c.556T>G