Canonical Allele Identifier: PA2826507077
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3016298
ClinVar RCV Id: RCV003876449

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Leu107Phe
CA378384038
NM_001269039.3:c.321A>C
CA378384042
NM_001269039.3:c.321A>T