Canonical Allele Identifier: PA658660008
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 448369
ClinVar RCV Id: RCV000517952 RCV002060260 RCV003159662
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Val1105Met
CA3498781
NM_024577.4:c.3313G>A