Canonical Allele Identifier: PA2827006984
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64986

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Glu449Lys
CA014970
NM_001318829.2:c.1345G>A