Canonical Allele Identifier: PA2829975178
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Gly676Val
CA035845
NM_021055.3:c.2027G>T