Allele Registry

Canonical Allele Identifier: PA2827250938

Gene: SHOC2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

49107

ClinVar RCV:

RCV000159109

RCV000766822

RCV000799563

RCV001004912

RCV001261147

RCV001813276

RCV002390134

ClinVar Variation:

40637

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311265.1:p.Glu25Gly	CA297172 NM_001324336.2:c.74A>G