Canonical Allele Identifier: PA2827018799
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468005
ClinVar Variation Id: 578164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Val1087Leu
CA276746154
NM_001318832.2:c.3259G>T
CA394286664
NM_001318832.2:c.3259G>C