Canonical Allele Identifier: PA2827006751
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Pro370Ser
CA014179
NM_001318829.2:c.1108C>T