Canonical Allele Identifier: PA2827009761
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1512761
ClinVar RCV Id: RCV002023196

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Phe1412Ser
CA394304382
NM_001318829.2:c.4235T>C