Canonical Allele Identifier: PA645431825
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 318307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ile247Val
CA056277
NM_000548.5:c.739A>G