Canonical Allele Identifier: PA2825184338
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1475211

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ser1002Tyr
CA394283809
NM_000548.5:c.3005C>A