Canonical Allele Identifier: PA2827018884
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Asp1110Val
CA319512
NM_001318832.2:c.3329A>T