Canonical Allele Identifier: PA2827251414
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 240838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Ile204Val
CA5689600
NM_001324337.2:c.610A>G