Allele Registry

Canonical Allele Identifier: PA658659938

Gene: SH3TC2 HGNC NCBI

ClinVar RCV:

RCV000520448

RCV000654163

RCV001332529

RCV002420317

ClinVar Variation:

450820

HGVS (amino-acid)	Matching Registered Transcripts
NP_078853.2:p.Ser265Phe	CA3499391 NM_024577.4:c.794C>T