Canonical Allele Identifier: PA2580369062
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2124031
ClinVar RCV Id: RCV003035713
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Lys216Ile
CA378386455
NM_007373.4:c.647A>T