Canonical Allele Identifier: PA2499290454
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1040454
ClinVar RCV Id: RCV001344105

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Tyr680Cys
CA3499072
NM_024577.4:c.2039A>G