Allele Registry

Canonical Allele Identifier: PA658660007

Gene: SH3TC2 HGNC NCBI

ClinVar Variation Id: 476906

HGVS (amino-acid)	Matching Registered Transcripts
NP_078853.2:p.Thr1098Ile	CA3498791 NM_024577.4:c.3293C>T