Allele Registry

Canonical Allele Identifier: PA113685

Gene: SH3TC2 HGNC NCBI

ClinVar RCV:

RCV000196497

RCV002288810

RCV002399744

ClinVar Variation:

216005

HGVS (amino-acid)	Matching Registered Transcripts
NP_078853.2:p.Arg529Gln	CA336470 NM_024577.4:c.1586_1587delinsAG