Allele Registry

Canonical Allele Identifier: PA1139755516

Gene: SH3TC2 HGNC NCBI

ClinVar RCV:

RCV001225215

RCV002290645

RCV002451529

RCV002497767

ClinVar Variation:

952984

HGVS (amino-acid)	Matching Registered Transcripts
NP_078853.2:p.Arg1171His	CA3498694 NM_024577.4:c.3512G>A