Canonical Allele Identifier: PA916023207
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Val78Ile
CA035477
NM_001318832.2:c.232G>A