Canonical Allele Identifier: PA2827251339
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1025311
ClinVar RCV Id: RCV001325614
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Ser85Phe
CA378383076
NM_001324337.2:c.254C>T