Canonical Allele Identifier: PA2826506978
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2770738
ClinVar RCV Id: RCV003540446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Gly35Arg
CA5689555
NM_001269039.3:c.103G>A
CA378381375
NM_001269039.3:c.103G>C