Allele Registry

Canonical Allele Identifier: PA645414246

Gene: SH3TC2 HGNC NCBI

ClinVar Variation Id: 284014

HGVS (amino-acid)	Matching Registered Transcripts
NP_078853.2:p.Arg861Trp	CA3498966 NM_024577.4:c.2581C>T