Allele Registry

Canonical Allele Identifier: PA2827251020

Gene: SHOC2 HGNC NCBI

ClinVar Allele:

1046442

ClinVar RCV:

RCV001362259

RCV001813593

ClinVar Variation:

1053860

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311265.1:p.Gly143Glu	CA5689589 NM_001324336.2:c.428G>A