Canonical Allele Identifier: PA2825434959
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg308Trp
CA056666
NM_001077183.3:c.922C>T