Canonical Allele Identifier: PA2827013873
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65104

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Pro678Ser
CA017740
NM_001318831.2:c.2032C>T