Canonical Allele Identifier: PA2580462746
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2129943
ClinVar RCV Id: RCV003050260

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Ser608Asn
CA361667655
NM_024577.4:c.1823G>A