Canonical Allele Identifier: PA2825435343
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 383175

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.His435Tyr
CA029254
NM_001077183.3:c.1303C>T