Canonical Allele Identifier: PA2826507101
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1310782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Ile114Met
CA378384376
NM_001269039.3:c.342A>G