Canonical Allele Identifier: PA2827011055
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207715

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Val412Met
CA319441
NM_001318829.2:c.1234G>A