Canonical Allele Identifier: PA645414212
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 407266
ClinVar RCV Id: RCV000458241 RCV000762176 RCV001174038 RCV002523308
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Arg536Gln
CA3499150
NM_024577.4:c.1607G>A