Allele Registry

Canonical Allele Identifier: PA645414346

Gene: SH3TC2 HGNC NCBI

ClinVar Variation Id: 287406

HGVS (amino-acid)	Matching Registered Transcripts
NP_078853.2:p.Ile1253Val	CA3498635 NM_024577.4:c.3757A>G