Canonical Allele Identifier: PA2828420227
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207750

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Glu1301Lys
CA050233
NM_001370405.1:c.3901G>A