Canonical Allele Identifier: PA2827012955
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 385710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ala423Val
CA16608037
NM_001318831.2:c.1268C>T