Canonical Allele Identifier: PA2827019849
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ser1393Phe
CA050898
NM_001318832.2:c.4178C>T