Canonical Allele Identifier: PA355816
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 219388
ClinVar RCV Id: RCV000205496 RCV000235753 RCV000289039 RCV000726668 RCV001095079 RCV002372193 RCV004541285 RCV001173160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Val230Ala
CA349654
NM_024577.4:c.689T>C