Canonical Allele Identifier: PA658659951
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 448363
ClinVar RCV Id: RCV000516825 RCV000798572 RCV002383996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Arg440His
CA3499200
NM_024577.4:c.1319G>A