Canonical Allele Identifier: PA658811736
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 543425
ClinVar RCV Id: RCV000654184 RCV001155698 RCV001155699 RCV002422422 RCV003126893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Ala673Thr
CA3499076
NM_024577.4:c.2017G>A