Canonical Allele Identifier: PA2499290418
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000680
ClinVar RCV Id: RCV001296838 RCV002411944
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Arg641Cys
CA3499093
NM_024577.4:c.1921C>T