Canonical Allele Identifier: PA658680266
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468016

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg115His
CA046888
NM_000548.5:c.344G>A