Canonical Allele Identifier: PA122363
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg905Gly
CA017936
NM_000548.5:c.2713C>G