Canonical Allele Identifier: PA658659938
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 450820
ClinVar RCV Id: RCV000520448 RCV000654163 RCV001332529 RCV002420317
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Ser265Phe
CA3499391
NM_024577.4:c.794C>T