Canonical Allele Identifier: PA658659998
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 476903
ClinVar RCV Id: RCV000547987 RCV001157279 RCV001157280 RCV003488695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Arg1012Trp
CA3498872
NM_024577.4:c.3034C>T