Canonical Allele Identifier: PA2825572030
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Val67Ile
CA035477
NM_001114382.3:c.199G>A