Canonical Allele Identifier: PA2827251283
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2077589
ClinVar RCV Id: RCV002976576
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Ser11Pro
CA378380423
NM_001324337.2:c.31T>C