Canonical Allele Identifier: PA2829981126
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49830

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Ser1411Gly
CA020332
NM_021055.3:c.4231A>G