Canonical Allele Identifier: PA2827014122
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 649255

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ser755Thr
CA394283753
NM_001318831.2:c.2264G>C