Canonical Allele Identifier: PA2499290453
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1038311
ClinVar RCV Id: RCV001341601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Val672Ala
CA361667261
NM_024577.4:c.2015T>C