Canonical Allele Identifier: PA658659989
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 476901
ClinVar RCV Id: RCV000534509 RCV000998462 RCV001173819 RCV002431715 RCV003387882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Arg861Gln
CA3498964
NM_024577.4:c.2582G>A