Canonical Allele Identifier: PA2825572117
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Arg93Trp
CA041936
NM_001114382.3:c.277C>T