Canonical Allele Identifier: PA658805119
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 536087

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Glu1805Lys
CA055360
NM_000548.5:c.5413G>A