Canonical Allele Identifier: PA2826506956
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1760674

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Lys26Arg
CA5689550
NM_001269039.3:c.77A>G