Allele Registry

Canonical Allele Identifier: PA2827251010

Gene: SHOC2 HGNC NCBI

ClinVar Allele:

179141

ClinVar RCV:

RCV000466484

RCV000763645

RCV001813417

RCV002262761

RCV002336368

ClinVar Variation:

181527

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311265.1:p.Ile119Val	CA297175 NM_001324336.2:c.355A>G