Canonical Allele Identifier: PA658805117
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 514715

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Gln1779Arg
CA055149
NM_000548.5:c.5336A>G