Canonical Allele Identifier: PA2828093991
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ser1299Leu
CA050423
NM_001363528.2:c.3896C>T