Canonical Allele Identifier: PA2825434303
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg93Trp
CA041936
NM_001077183.3:c.277C>T