Canonical Allele Identifier: PA355084
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 219741
ClinVar RCV Id: RCV000203817 RCV001153404 RCV001153403 RCV002381703 RCV004530221 RCV000235858 RCV000789697 RCV001722118
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Gln46Pro
CA348097
NM_024577.4:c.137A>C