Canonical Allele Identifier: PA645431985
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237964

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg458Gln
CA10583294
NM_000548.5:c.1373G>A