Canonical Allele Identifier: PA2580369025
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2141254

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Lys36Arg
CA5689556
NM_007373.4:c.107A>G