Canonical Allele Identifier: PA2827019499
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207750

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Glu1288Lys
CA050233
NM_001318832.2:c.3862G>A