Canonical Allele Identifier: PA658659953
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 452652
ClinVar RCV Id: RCV000523748 RCV000654135 RCV001027477 RCV002384018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Pro442Leu
CA3499197
NM_024577.4:c.1325C>T