Canonical Allele Identifier: PA2827251066
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2180360
ClinVar RCV Id: RCV002619217
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311265.1:p.Ile211Met
CA378386336
NM_001324336.2:c.633C>G