Canonical Allele Identifier: PA2827251317
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2715205
ClinVar RCV Id: RCV003539678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Asp52Tyr
CA378381861
NM_001324337.2:c.154G>T