Canonical Allele Identifier: PA2825574432
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406028

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Leu764Met
CA16615073
NM_001114382.3:c.2290C>A