Canonical Allele Identifier: PA891853065
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 578843
ClinVar RCV Id: RCV000701971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Arg997Trp
CA3498882
NM_024577.4:c.2989C>T