Canonical Allele Identifier: PA2829980247
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207750

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Glu1301Lys
CA050233
NM_021055.3:c.3901G>A