Canonical Allele Identifier: PA355725
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 220296
ClinVar RCV Id: RCV001081115 RCV001156005 RCV001153405 RCV000205289 RCV002415868 RCV000789695 RCV004530230
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Thr27Ala
CA349459
NM_024577.4:c.79A>G