Canonical Allele Identifier: PA2828414088
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207750

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Glu1300Lys
CA050233
NM_001370404.1:c.3898G>A