Canonical Allele Identifier: PA2573284474
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1366657
ClinVar RCV Id: RCV001930183

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Pro1114Ala
CA3498760
NM_024577.4:c.3340C>G