Canonical Allele Identifier: PA2825574410
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237986

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ser758Cys
CA10583307
NM_001114382.3:c.2273C>G