Canonical Allele Identifier: PA2580462791
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2173900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Arg1002Ser
CA3498879
NM_024577.4:c.3006G>T
CA361665138
NM_024577.4:c.3006G>C