Allele Registry

Canonical Allele Identifier: PA2827251103

Gene: SHOC2 HGNC NCBI

ClinVar RCV:

RCV000203043

RCV002272173

RCV002273987

RCV002515502

RCV003407717

ClinVar Variation:

218698

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311265.1:p.Gln269Arg	CA249249 NM_001324336.2:c.806A>G