Canonical Allele Identifier: PA2825438547
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg1403His
CA16614762
NM_001077183.3:c.4208G>A