Canonical Allele Identifier: PA2827012205
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Pro219Ser
CA014179
NM_001318831.2:c.655C>T