Canonical Allele Identifier: PA645414179
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 374659
ClinVar RCV Id: RCV000416281 RCV000654078 RCV001153291 RCV001153292 RCV001173823 RCV002392943
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Pro251Ser
CA3499401
NM_024577.4:c.751C>T