Canonical Allele Identifier: PA916024038
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238007

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Gln977Glu
CA044006
NM_001318832.2:c.2929C>G