Canonical Allele Identifier: PA2829717784
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3161865
ClinVar RCV Id: RCV004451211
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Lys209Thr
CA378386296
NM_007373.4:c.626A>C