Canonical Allele Identifier: PA2580369022
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1760674

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Lys26Arg
CA5689550
NM_007373.4:c.77A>G