Canonical Allele Identifier: PA645414214
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 351913
ClinVar RCV Id: RCV000310013 RCV000490113 RCV000525499 RCV001095013 RCV001173167 RCV002402071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Asn574Ser
CA3499137
NM_024577.4:c.1721A>G