Canonical Allele Identifier: PA2826507107
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181527

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Ile119Val
CA297175
NM_001269039.3:c.355A>G