Allele Registry

Canonical Allele Identifier: PA645414219

Gene: SH3TC2 HGNC NCBI

ClinVar RCV:

RCV000232630

ClinVar Variation:

241501

HGVS (amino-acid)	Matching Registered Transcripts
NP_078853.2:p.Arg621Cys	CA3499103 NM_024577.4:c.1861C>T