Canonical Allele Identifier: PA2825439552
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49471

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg1676Trp
CA022213
NM_001077183.3:c.5026C>T