Canonical Allele Identifier: PA2828412003
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Arg680Gln
CA035970
NM_001370404.1:c.2039G>A