Allele Registry

Canonical Allele Identifier: PA658811791

Gene: SH3TC2 HGNC NCBI

ClinVar RCV:

RCV000654114

ClinVar Variation:

543366

HGVS (amino-acid)	Matching Registered Transcripts
NP_078853.2:p.Arg1171Pro	CA361664220 NM_024577.4:c.3512G>C