Canonical Allele Identifier: PA658659939
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 451739
ClinVar RCV Id: RCV000523668 RCV000795540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Arg272Cys
CA3499373
NM_024577.4:c.814C>T