Canonical Allele Identifier: PA658659976
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 476894
ClinVar RCV Id: RCV000541890 RCV002448797
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Asp752Asn
CA3499038
NM_024577.4:c.2254G>A