Allele Registry

Canonical Allele Identifier: PA355725

Gene: SH3TC2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

221616

ClinVar RCV:

RCV000205289

RCV000789695

RCV001081115

RCV001153405

RCV001156005

RCV002415868

RCV004530230

ClinVar Variation:

220296

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_078853.2:p.Thr27Ala	CA349459 NM_024577.4:c.79A>G