Canonical Allele Identifier: PA334026
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 188089
ClinVar RCV Id: RCV000237055 RCV000713265 RCV001082893 RCV000789576 RCV000987610 RCV001157181 RCV002453563 RCV004535140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Asp1229Val
CA334024
NM_024577.4:c.3686A>T