Canonical Allele Identifier: PA2829981147
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535870

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Arg1414Trp
CA051001
NM_021055.3:c.4240C>T