Canonical Allele Identifier: PA2828095371
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49471

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Arg1677Trp
CA022213
NM_001363528.2:c.5029C>T