Allele Registry

Canonical Allele Identifier: PA658659987

Gene: SH3TC2 HGNC NCBI

ClinVar Variation Id: 476899

HGVS (amino-acid)	Matching Registered Transcripts
NP_078853.2:p.Gly843Val	CA361666180 NM_024577.4:c.2528G>T