Canonical Allele Identifier: PA658811683
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 543415
ClinVar RCV Id: RCV000654173 RCV000857157 RCV001153290 RCV001092867 RCV002424545 RCV001153289 RCV004527713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Thr277Met
CA3499369
NM_024577.4:c.830C>T