Canonical Allele Identifier: PA645414163
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 414373
ClinVar RCV Id: RCV000471681 RCV000508286 RCV001173159 RCV002383875
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Asp25Tyr
CA3499635
NM_024577.4:c.73G>T