Canonical Allele Identifier: PA2827251037
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 373090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Met173Val
CA16042684
NM_001324336.2:c.517A>G