Canonical Allele Identifier: PA658681215
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Pro1450Ala
CA050903
NM_000548.5:c.4348C>G