Canonical Allele Identifier: PA2825438196
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ser1298Leu
CA050423
NM_001077183.3:c.3893C>T