Allele Registry

Canonical Allele Identifier: PA645414330

Gene: SH3TC2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000214292

RCV000355518

RCV000473910

RCV001095006

RCV001173826

RCV001352888

RCV001549281

RCV002450641

RCV004529380

ClinVar Variation:

234414

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_078853.2:p.Arg1127Gln	CA3498756 NM_024577.4:c.3380G>A