Canonical Allele Identifier: PA2828415550
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49471

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Arg1699Trp
CA022213
NM_001370404.1:c.5095C>T