Canonical Allele Identifier: PA645414224
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 351908
ClinVar RCV Id: RCV000268641 RCV000360932 RCV001030761 RCV001706582 RCV001095110
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Arg648Trp
CA3499088
NM_024577.4:c.1942C>T