Canonical Allele Identifier: PA334116
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 188129
ClinVar RCV Id: RCV000167994 RCV000297914 RCV000336302 RCV001174042 RCV002321674
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Arg11Trp
CA334114
NM_024577.4:c.31C>T