Canonical Allele Identifier: PA2828094342
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Arg1404His
CA16614762
NM_001363528.2:c.4211G>A