Canonical Allele Identifier: PA2825184319
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 664836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ser999Asn
CA043671
NM_000548.5:c.2996G>A