Allele Registry

Canonical Allele Identifier: PA658811683

Gene: SH3TC2 HGNC NCBI

ClinVar RCV:

RCV000654173

RCV000857157

RCV001092867

RCV001153289

RCV001153290

RCV002424545

RCV004527713

ClinVar Variation:

543415

HGVS (amino-acid)	Matching Registered Transcripts
NP_078853.2:p.Thr277Met	CA3499369 NM_024577.4:c.830C>T