Allele Registry

Canonical Allele Identifier: PA645414194

Gene: SH3TC2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

265353

ClinVar RCV:

RCV000558978

RCV000723677

RCV000789696

RCV001157494

RCV001157495

RCV001706410

RCV002379107

RCV003319193

ClinVar Variation:

281116

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_078853.2:p.Ser433Leu	CA3499208 NM_024577.4:c.1298C>T