Canonical Allele Identifier: PA916076792
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 694975

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Arg605Cys
CA3499118
NM_024577.4:c.1813C>T