Canonical Allele Identifier: PA239665
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 193930
ClinVar RCV Id: RCV000236423 RCV000724178 RCV001157383 RCV001085590 RCV001157384 RCV001173837 RCV002408756 RCV004535197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Arg621His
CA239663
NM_024577.4:c.1862G>A