Canonical Allele Identifier: PA2827251366
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181527

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Ile119Val
CA297175
NM_001324337.2:c.355A>G