Canonical Allele Identifier: PA645414203
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 407267
ClinVar RCV Id: RCV000462842 RCV000507530 RCV001173158 RCV002393104 RCV004533178
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Thr495Ala
CA3499167
NM_024577.4:c.1483A>G