Allele Registry

Canonical Allele Identifier: PA645414180

Gene: SH3TC2 HGNC NCBI

ClinVar Variation Id: 245804

HGVS (amino-acid)	Matching Registered Transcripts
NP_078853.2:p.Tyr279Cys	CA3499364 NM_024577.4:c.836A>G