Canonical Allele Identifier: PA2827250966
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2079868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Ser58Asn
CA5689560
NM_001324336.2:c.173G>A