Canonical Allele Identifier: PA2827006188
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Arg159Trp
CA022695
NM_001318829.2:c.475C>T