Allele Registry

Canonical Allele Identifier: PA645414236

Gene: SH3TC2 HGNC NCBI

ClinVar Variation Id: 245704

HGVS (amino-acid)	Matching Registered Transcripts
NP_078853.2:p.Glu769Gly	CA3499028 NM_024577.4:c.2306A>G