Canonical Allele Identifier: PA2826506954
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 40637
ClinVar RCV Id: RCV000799563 RCV000766822 RCV000159109 RCV001004912 RCV001261147 RCV001813276 RCV002390134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Glu25Gly
CA297172
NM_001269039.3:c.74A>G