Canonical Allele Identifier: PA2828413353
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406072

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Arg1083Trp
CA046408
NM_001370404.1:c.3247C>T