Canonical Allele Identifier: PA658681362
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468145

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Asn1731Lys
CA394314174
NM_000548.5:c.5193C>A
CA394314180
NM_000548.5:c.5193C>G