Canonical Allele Identifier: PA2827019926
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Arg1414His
CA16614762
NM_001318832.2:c.4241G>A