Canonical Allele Identifier: PA1139755011
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 960691
ClinVar RCV Id: RCV001234264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Asp681Tyr
CA361667204
NM_024577.4:c.2041G>T