Allele Registry

Canonical Allele Identifier: PA645414187

Gene: SH3TC2 HGNC NCBI

ClinVar Variation Id: 351915

HGVS (amino-acid)	Matching Registered Transcripts
NP_078853.2:p.Arg369Cys	CA3499292 NM_024577.4:c.1105C>T