Allele Registry

Canonical Allele Identifier: PA658660012

Gene: SH3TC2 HGNC NCBI

ClinVar RCV:

RCV000517446

RCV000754746

RCV000790335

RCV000805465

RCV001814180

RCV003483649

ClinVar Variation:

448370

HGVS (amino-acid)	Matching Registered Transcripts
NP_078853.2:p.Arg1171Cys	CA3498696 NM_024577.4:c.3511C>T