Canonical Allele Identifier: PA658680273
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468038

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Lys125Arg
CA048294
NM_000548.5:c.374A>G