Canonical Allele Identifier: PA645414194
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 281116
ClinVar RCV Id: RCV000558978 RCV000723677 RCV000789696 RCV001157494 RCV001157495 RCV001706410 RCV002379107 RCV003319193
JSON-LD

Amino-acid Alleles

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