Canonical Allele Identifier: PA645414281
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246193
ClinVar RCV Id: RCV000236841 RCV000477370 RCV000767114 RCV000765819 RCV001173155 RCV002436061
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Glu985Gly
CA3498889
NM_024577.4:c.2954A>G