Canonical Allele Identifier: PA645414330
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 234414
ClinVar RCV Id: RCV000214292 RCV000355518 RCV000473910 RCV001173826 RCV001352888 RCV001095006 RCV001549281 RCV002450641 RCV004529380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Arg1127Gln
CA3498756
NM_024577.4:c.3380G>A