Canonical Allele Identifier: PA2829977403
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12404

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Arg905Trp
CA017942
NM_021055.3:c.2713C>T