Allele Registry

Canonical Allele Identifier: PA342386

Gene: SH3TC2 HGNC NCBI

ClinVar RCV:

RCV000790208

ClinVar Variation:

21698

HGVS (amino-acid)	Matching Registered Transcripts
NP_078853.2:p.Arg1109Pro	CA342384 NM_024577.4:c.3326G>C