Canonical Allele Identifier: PA916023526
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64986

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Glu509Lys
CA014970
NM_001318832.2:c.1525G>A