Canonical Allele Identifier: PA645455643
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 373090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Met173Val
CA16042684
NM_007373.4:c.517A>G