Canonical Allele Identifier: PA2828415253
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Val1629Phe
CA021508
NM_001370404.1:c.4885G>T