Canonical Allele Identifier: PA2829970975
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65349

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Glu114Lys
CA019111
NM_021055.3:c.340G>A